Importation of Swine and Swine Products From the European Union, 17928-17940 [05-7013]
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17928
Proposed Rules
Federal Register
Vol. 70, No. 67
Friday, April 8, 2005
This section of the FEDERAL REGISTER
contains notices to the public of the proposed
issuance of rules and regulations. The
purpose of these notices is to give interested
persons an opportunity to participate in the
rule making prior to the adoption of the final
rules.
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
9 CFR Parts 93, 94, and 98
[Docket No. 02–046–1]
RIN 0579–AB79
Importation of Swine and Swine
Products From the European Union
Animal and Plant Health
Inspection Service, USDA.
ACTION: Proposed rule.
AGENCY:
SUMMARY: We are proposing to amend
the regulations for importing animals
and animal products into the United
States to apply a uniform set of
importation requirements related to
classical swine fever (CSF) to a region
consisting of all of the 15 Member States
of the European Union (EU) that
comprised the EU as of April 30, 2004
(the EU–15) and prohibit for a specified
period of time the importation of live
swine and swine products from any area
in the EU–15 that is identified by the
veterinary authorities of the region as a
restricted zone. We believe these
changes are necessary to help prevent
the introduction of CSF into the United
States while increasing our
responsiveness to changes in the CSF
situation in the EU.
DATES: We will consider all comments
that we receive on or before June 7,
2005.
You may submit comments
by any of the following methods:
• EDOCKET: Go to https://
www.epa.gov/feddocket to submit or
view public comments, access the index
listing of the contents of the official
public docket, and to access those
documents in the public docket that are
available electronically. Once you have
entered EDOCKET, click on the ‘‘View
Open APHIS Dockets’’ link to locate this
document.
• Postal Mail/Commercial Delivery:
Please send four copies of your
ADDRESSES:
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comment (an original and three copies)
to Docket No. 02–046–1, Regulatory
Analysis and Development, PPD,
APHIS, Station 3C71, 4700 River Road
Unit 118, Riverdale, MD 20737–1238.
Please state that your comment refers to
Docket No. 02–046–1.
• Federal eRulemaking Portal: Go to
https://www.regulations.gov and follow
the instructions for locating this docket
and submitting comments.
Reading Room: You may read any
comments that we receive on this
docket in our reading room. The reading
room is located in room 1141 of the
USDA South Building, 14th Street and
Independence Avenue SW.,
Washington, DC. Normal reading room
hours are 8 a.m. to 4:30 p.m., Monday
through Friday, except holidays. To be
sure someone is there to help you,
please call (202) 690–2817 before
coming.
Other Information: You may view
APHIS documents published in the
Federal Register and related
information on the Internet at https://
www.aphis.usda.gov/ppd/rad/
webrepor.html.
FOR FURTHER INFORMATION CONTACT: Dr.
Chip Wells, Senior Staff Veterinarian,
Regionalization Evaluation Services
Staff, National Center for Import and
Export, VS, APHIS, 4700 River Road
Unit 38, Riverdale, MD 20737–1231;
(301) 734–4356.
SUPPLEMENTARY INFORMATION:
Background
The Animal and Plant Health
Inspection Service (APHIS) of the
United States Department of Agriculture
(USDA or the Department) regulates the
importation of animals and animal
products into the United States to guard
against the introduction of animal
diseases not currently present or
prevalent in this country. The
regulations in 9 CFR part 94 (referred to
below as the regulations) prohibit or
restrict the importation of specified
animals and animal products to prevent
the introduction into the United States
of various animal diseases, including
classical swine fever (CSF), rinderpest,
foot-and-mouth disease, bovine
spongiform encephalopathy, swine
vesicular disease, and African swine
fever.
Sections 94.9 and 94.10 of the
regulations state that CSF is known to
exist in all regions of the world, except
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for those regions listed in §§ 94.9(a) and
94.10(a). The importation of live swine
and swine products from regions not
recognized as free of CSF is restricted or
prohibited. In addition, the importation
of live swine and swine products from
a region consisting of certain Member
States and portions of Member States of
the European Union (EU) is restricted
with regard to CSF, even though that
region is listed as free of the disease.
The restrictions on imports from that
region were established in a final rule
published in the Federal Register on
April 7, 2003 (68 FR 16922–16941,
Docket No. 98–090–5).
We based our final rule primarily on
two risk analyses conducted by
APHIS.1 2 The risk analyses examined a
region consisting of EU countries
(Member States) that the European
Commission (EC) asked us to recognize
as free of CSF. (The EC is the EU
institution responsible for representing
the EU as a whole. It proposes
legislation, policies, and programs of
action and implements decisions of the
EU Parliament and Council.) The
Member States identified were Austria,
Belgium, France, Germany, Greece,
Italy, Luxembourg, the Netherlands,
Portugal, and Spain. Five other EU
Member States—Denmark, Finland, the
Republic of Ireland, Sweden, and the
United Kingdom—were already
recognized by APHIS as being free of
CSF.
The first risk analysis was made
available to the public in 1999 at the
time of publication in the Federal
Register of the proposed rule (64 FR
34155–34168, Docket No. 98–090–1)
upon which we based our April 2003
final rule. The second risk analysis was
released in 2002 for public comment (67
FR 22388–22389, Docket No. 98–090–2)
and represented a revision and
supplementation of the 1999 risk
analysis. Data used in both risk analyses
represented events that occurred during
a CSF epidemic in Europe during 1997
and 1998. That outbreak is considered
to be the most severe CSF epidemic ever
experienced in Europe. Both risk
analyses are available by calling or
writing to the person listed in this
1 Biological Risk Analysis: Risk assessment and
management options for imports of swine and
swine products from the European Union—June 2,
1999.
2 Risk Analysis for Importation of Classical Swine
Fever Virus in Swine and Swine Products from the
European Union—December 2000.
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document under FOR FURTHER
INFORMATION CONTACT. The analyses are
also available on the Internet at https://
www.aphis.usda.gov/vs/ncie/regrequest.html. At the bottom of that Web
site page, click on ‘‘Information
previously submitted by Regions
requesting export approval and
supporting documentation.’’ At the next
screen, click on the triangle beside
‘‘European Union/Not Specified/
Classical Swine Fever,’’ then click on
the triangle beside ‘‘Response by
APHIS,’’ which will reveal links to the
risk analyses.
The analyses took into account,
among other things, the CSF history of
the EU region consisting of the 10
Member States in the EC’s request, the
CSF history of countries adjacent to the
region, the veterinary infrastructure and
policies of the region, and the historical
volumes of imports into the United
States of breeding swine, swine semen,
and pork and pork products from the
region.
Based on the analyses, we considered
it necessary to establish certain
mitigation measures for the importation
of live swine, pork and pork products,
and swine semen from the region.
Although there were no CSF outbreaks
in EU domestic swine within the
defined region at the time, the risk
analyses assumed that, because CSF was
endemic in wild boar in several parts of
the EU, it was likely CSF would
continue to occur in domestic swine in
the region. Further, the risk analyses
considered the open borders among EU
Member States. To address these
situations, the final rule required that
commodities from the region of the EU
that was considered to be unaffected
with CSF be segregated from those from
CSF-affected regions of the EU and other
CSF-affected regions, and that measures
be taken to ensure that donor boars
providing semen for export to the
United States are truly free of CSF.
These requirements are described below
under the heading ‘‘Importation
Conditions Established in April 2003.’’
Importation Conditions Established in
April 2003
Specifically, our April 2003 final rule
required that the following conditions
be met before the commodity in
question could be imported into the
United States (in the absence of any
other diseases of swine that would
otherwise prohibit importation):
• For pork and pork products: (1) The
articles have not been commingled with
pork or pork products derived from
swine that have been in a region listed
at the time as one in which CSF is
known to exist; (2) the swine from
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which the pork or pork products were
derived have not lived in a region listed
at the time as one in which CSF is
known to exist, and have not transited
such a region unless moved directly
through the region in a sealed means of
conveyance with the seal determined to
be intact upon arrival at the point of
destination; and (3) the articles are
accompanied by a certificate, issued by
an official of the national government of
the region of origin, stating that the
above provisions have been met.
• For breeding swine: The swine (1)
have never lived in a region listed at the
time as one in which CSF is known to
exist; (2) have never transited such a
region unless moved directly through
the region in a sealed means of
conveyance with the seal determined to
be intact upon arrival at the point of
destination; and (3) have never been
commingled with swine that have been
in a region listed at the time as one in
which CSF is known to exist.
Additionally, no equipment or materials
used in transporting the swine may have
previously been used for transporting
swine ineligible for export to the United
States unless the equipment or materials
first were cleaned and disinfected.
Lastly, the swine have to be
accompanied by a certificate, issued by
a salaried veterinary officer of the
national government of the country of
origin, stating that the above provisions
have been met.
• For swine semen: The donor boar
meets the same conditions as those
listed above for breeding swine.
Additionally, the following conditions
must be met: (1) The semen comes from
a semen collection center approved for
export by the veterinary services of the
national government of the country of
origin; (2) the donor boar is held in
isolation for at least 30 days prior to
entering the semen collection center,
and, no more than 30 days prior to being
held in isolation, is tested with negative
results using a CSF test approved by the
Office International des Epizooties (OIE)
[also referred to as the World
Organisation of Animal Health]; and (3)
the donor boar is observed by the semen
collection center veterinarian while at
the center (including at least a 40-day
holding period at the center following
collection of the semen) and, along with
all other swine at the center, exhibits no
clinical signs of CSF.
Under these conditions, we estimated
that the risk of introducing CSF through
imports from the defined region would
be as follows:
• By importing breeding swine, most
likely one incursion in an average of
33,670 years.
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• By importing fresh pork, most likely
one incursion in an average of 22,676
years.
• By importing swine semen, most
likely one incursion in an average of
8,090 years.
APHIS considered each of these risks
to be low.
We continue to consider the
mitigation measures established in our
April 2003 final rule to be necessary for
the importation of breeding swine, pork
and pork products, and swine semen
from the EU region we recognized in
that final rule, and to France and Spain,
which were added to that region
following publication of the April 2003
final rule in a final rule published on
April 20, 2004 (69 FR 21042–21047,
Docket No. 98–090–7). Under this
proposed rule, those requirements
would continue to apply.
Additionally, we are proposing to
apply the measures established in our
April 2003 final rule to importations
from five additional EU Member States
whose exports to the United States are
free of CSF-related restrictions
(Denmark, Finland, the Republic of
Ireland, Sweden, and the United
Kingdom [consisting of England,
Scotland, Wales, the Isle of Man, and
Northern Ireland]), as well as to
Luxembourg (which is currently listed
as a region in which CSF exists, due to
an outbreak of the disease following our
June 1999 proposal) and all of Germany
and Italy. Currently, only portions of
Germany and Italy are recognized as free
of CSF in our regulations. We would
apply the same mitigation measures to
each of the areas described above
because we would recognize the
combination of all of those areas of the
EU as a single region of low-risk for
CSF, discussed below. The region
would be comprised of the 15 Member
States comprising the EU as of April 30,
2004, which we refer to as the European
Union–15 (EU–15). We would add a
definition of European Union–15 (EU–
15) to §§ 93.500, 94.0, and 98.30.
We discuss below, under the heading
‘‘Uniform Conditions for Imports from
the EU–15,’’ our proposed application of
uniform import conditions to the EU–15
with regard to CSF. We then discuss the
reasons we believe the EU–15 qualifies
as a region of low-risk for CSF under the
heading ‘‘Basis for Recognition of an EU
Region.’’
Uniform Conditions for Imports From
the EU–15
As noted above, we are proposing to
recognize a single region for CSF (the
EU–15) that would consist of the
following areas: (1) That region of the
EU we now recognize as being free of
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CSF but from which imports of swine
and swine products are subject to
specified restrictions; (2) Denmark,
Finland, the Republic of Ireland,
Sweden, and the United Kingdom
(consisting of England, Scotland, Wales,
the Isle of Man, and Northern Ireland);
and (3) Luxembourg and all of Germany
and Italy. Currently, only portions of
Germany and Italy are recognized as free
of CSF in our regulations.
In our April 2003 final rule, we did
not include Denmark, Finland, the
Republic of Ireland, Sweden, and the
United Kingdom in the EU region we
defined as free of classical swine fever
but from which the importation of
swine and swine products are subject to
certain restrictions. Those five Member
States had already been recognized in
previous rulemakings as regions in
which CSF is not known to exist and
from which swine and swine products
may be imported into the United States
without restriction related to CSF. We
continued to treat those Member States
in the same way we had been treating
them since the time we recognized them
as free of CSF; that is, we did not apply
to them the additional mitigation
measures we were applying to the EU
region we recognized in the April 2003
final rule.
However, because we had recognized
those five Member States as free of CSF
before the EU was established, the
evaluations we had conducted that
supported such a classification of
freedom did not take into account the
opening of national borders within the
EU and the possibility that the five CSFfree Member States would trade freely
with EU Member States that we
considered CSF-affected.
As part of the EU, those five Member
States carry out trade with the rest of the
EU under what is essentially an openborder trading policy. There is no
substantive difference between the way
trade is carried out within the EU by
those five Member States compared to
the way it is carried out by other
Member States. Because of these openborder policies, we believe the CSF risk
from the five member States must be
considered the same as from the EU
region we recognized as subject to
additional mitigation measures in our
April 2003 final rule, and the same
importation conditions would be
applied to both areas under this
proposed rule.
Additionally, we are proposing to
apply those importation conditions to
parts of the EU that we have not yet
recognized as CSF-free. In our April
2003 final rule, we excluded certain
parts of the EU—in some cases entire
Member States—from the region we
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recognized as CSF-free, either because
those areas were not eligible for
recognition as CSF-free at the time we
published the proposal for our April
2003 final rule, or because they
experienced an outbreak of CSF in
domestic swine following publication of
that proposed rule. Those areas
included all of France and Spain—
which have since been added to the
region of the EU we consider free of CSF
with restrictions—all of Luxembourg,
and parts of Germany and Italy. In
Germany, we excluded the following
kreis: the Kreis Uckermark in the Land
of Brandenburg; the Kreis Oldenberg,
the Kreis Soltau-Fallingbostel, and the
Kreis Vechta in the Land of Lower
Saxony; the Kreis Heinsberg and the
Kreis Warendorf in the Land of
Northrhine-Westphalia; the Kreis
Bernkastel-Wittlich, the Kreis Bitburg¨
Prum, the Kreis Donnersbergkreis, the
¨
Kreis Rhein-Hunsruche, the Kreis
¨
Sudliche Weinstrasse, and the Kreis
Trier-Saarburg in the Land of Rhineland
Palatinate; and the Kreis Altmarkkreis
in the Land of Saxony-Anhalt. In Italy,
we excluded the Regions of EmiliaRomagna, Piemonte, and Sardegna.
Whether we excluded an entire
Member State or a smaller
administrative unit depended on
whether we had identified in the June
1999 proposed rule the administrative
unit we would recognize as a region
within a particular Member State in the
event of a CSF outbreak. We had
identified such administrative units for
Germany and Italy (the ‘‘kreis’’ in
Germany and the ‘‘region’’ in Italy), but
not for the other Member States of the
EU.
We are now proposing to apply the
certification requirements established
by our April 2003 final rule to all the
areas in Italy and Germany listed above
and to Luxembourg. In addition, we
would require the EC to certify that
commodities (breeding swine, swine
semen, and fresh pork and pork
products) are not exported from—and
have not been commingled with swine
from—restricted zones in the EU during
the following time periods: (1) A period
of 6 months after the last case of CSF in
domestic swine in the restricted zone; or
(2) until restrictions put in place by the
EU because of CSF in wild boar in the
restricted zone are released. We
consider this action warranted because
we consider the EU to be an
homogeneous region of low CSF risk
(although one in which CSF outbreaks
may continue to occur) and because the
EC has appropriate control measures in
place to mitigate the risk of continuing
outbreaks.
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We consider the EU to be
homogeneous with regard to CSF
despite the fact that we have treated
certain kreis in Germany and Regions in
Italy slightly differently from the rest of
those countries during our rulemaking
process. Our June 1999 proposed rule
excluded three kreis in Germany and
three Regions in Italy from
consideration as part of the region
recognized in our April 2003 final rule.
Because these areas had experienced
outbreaks within 6 months before
collection of data for the 1999 risk
analysis, the model excluded
consideration of exports from those
areas. Exclusion of those areas was a
policy decision based on the
regionalization approach being used by
APHIS at the time.
However, the model used for the risk
analysis was based on the assumption
that outbreaks would continue to occur
in the EU. Even with this assumption,
the risk analysis concluded that the risk
of exporting CSF from the EU in
breeding swine, swine semen, and fresh
pork was low. Outbreaks did, in fact,
occur in some German kreis other than
the three excluded from the June 1999
proposed rule—as well as in France,
Spain, and Luxembourg, which were
subject to the June 1999 proposed rule—
and to provide the public an
opportunity to comment upon the
outbreaks, we did not include those
kreis and Member States in our April
2003 final rule. However, we consider
the CSF risk posed by commodities from
the German kreis and Italian Regions
that were excluded from the proposed
rule, as well as from those areas and
Member States that had outbreaks
subsequent to the proposed rule, to be
equivalent to the CSF risk from the
other EU–15 Member States (as
discussed above, in April 2004 we
added France and Spain to the EU
region we recognized in April 2003). We
consider the risk from the EU–15 as a
whole to be within the parameters of the
risk analysis, and believe the risk from
continuing CSF outbreaks in any part of
the EU–15 would be adequately
mitigated by the control mechanisms
implemented in the EU.
Thus, we are proposing to apply the
same import conditions for swine and
swine products with regard to CSF to a
region consisting of all of Austria,
Belgium, Denmark, Finland, France,
Germany, Greece, Italy, Luxembourg,
the Netherlands, Portugal, the Republic
of Ireland, Spain, Sweden, and the
United Kingdom. The conditions for
pork, pork products, and live swine
would be set forth in § 94.24. The
conditions for swine semen would be
set forth in § 98.38.
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The EU–15 as a Region of Low Risk for
CSF
In evaluating the CSF risk from
imports of breeding swine, swine
semen, and swine products from the
EU–15, we took into consideration the
following characteristics of that region:
• The region contains a known source
of CSF risk (e.g., infected wild boar) that
may spread the disease virus to EU
domestic swine, resulting in continuing
outbreaks of CSF in the region, but
veterinary officials in the region have
established risk mitigation measures
adequate to prevent widespread
exposure and establishment of the
disease;
• Specific mitigation measures in
place include surveillance,
epidemiological investigations,
diagnostic capability, and emergency
response capacity that are sufficient to
identify the disease, establish
appropriate control zones, and
implement all measures necessary to
effectively limit the spread of CSF from
the region; and
• Veterinary officials maintain
contingency plans defining proactive
approaches to CSF control: The
veterinary officials have sufficient legal
powers, a detailed chain-of-command,
and appropriate resources, including
emergency funds, laboratory staff,
equipment and infrastructure, to carry
out a rapid and effective eradication
campaign; there is an instruction
manual detailing all procedures,
instructions, and measures, including
emergency vaccination plans if deemed
necessary, to be implemented in the
event of a CSF outbreak; and
appropriate staff regularly receive
training and conduct drills in CSF
diagnosis, control measures, and
communication techniques.
Included in the EC request to APHIS
that resulted in our April 7, 2003, final
rule was a request that was made in the
context of the Veterinary Equivalence
Agreement (VEA) between the United
States and the EU, which was enacted
in 1998. (The stated objective of the
VEA is to facilitate trade in live animals
and animal products between the EU
and the United States by establishing a
mechanism for the recognition of
equivalence of sanitary measures,
consistent with the protection of public
and animal health, and improve
communication and cooperation on
sanitary issues.) The EC requested that
APHIS adopt the EC approach to
regionalization for CSF. This would
require APHIS to establish a new
approach to dealing with outbreaks of
CSF in the EU–15. As a result of our
review of the information provided, we
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are proposing to establish a new
approach that will adopt many elements
of the EC approach to dealing with
outbreaks of CSF in the EU–15. Rather
than responding to outbreaks through
rulemakings specific to each outbreak,
we are proposing in this document to
establish actions that we would take in
the event of a CSF outbreak in the
region. Our proposal and the way in
which it differs from current practice is
explained below. While the approach
we are proposing would, in this case,
apply specifically to the EU–15, we
would accept requests and supporting
information from other regions
interested in being considered for a
similar approach.
Currently, § 92.3 of the regulations
provides that whenever the EC
establishes a quarantine for a disease in
the EU in a region APHIS recognizes as
one in which the disease is not known
to exist and the EC imposes prohibitions
or other restrictions on the movement of
animals or animal products from the
quarantined area in the EU, such
animals and animal products are
prohibited importation into the United
States. Additionally, APHIS published a
final rule on May 4, 2004 (69 FR 25817–
25820, Docket No. 02–001–2) that
established procedures to follow when a
region that we recognize as free of an
animal disease experiences an outbreak
of that disease. If a region of the world
that is considered free of CSF
experiences an outbreak of CSF, APHIS
will prohibit or restrict immediately the
importation of live swine, fresh pork
and pork products, and swine semen
from that region into the United States.
We then may publish an interim rule in
the Federal Register as soon as possible
that removes that region from the lists
in §§ 94.9 and 94.10 of the regulations
of regions in which CSF does not exist
and that prohibits or restricts, by
regulation, the importation of live
swine, fresh pork and pork products,
and swine semen. We accept public
comment on the interim rule for a
specified period of time. If the outbreak
is eliminated in the region in question
and a sufficient amount of time passes
(generally defined as consistent with
OIE recommendations) to ensure that
the disease has been eradicated, we
evaluate the risk of resuming imports
from the region. If we believe the results
of the risk evaluation support
reinstatement of the region’s previous
CSF-free status and resumption of the
importation of the prohibited swine and
swine products into the United States,
we make the evaluation available to the
public and solicit public comment on it.
If, after considering the public
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comments, we still consider it
warranted to reinstate the region’s CSFfree status, we publish a final rule in the
Federal Register listing the region as
free of CSF, and we allow importations
of swine and swine products to resume.
We are proposing in this document
that, whenever an outbreak of CSF
occurs in the EU–15 and the competent
veterinary authority of the EU–15
Member State establishes a quarantined
area for CSF (also referred to in this
document as a ‘‘restricted zone’’), swine
and swine products will be prohibited
importation into the United States from
that zone. No action would be required
by APHIS; the prohibition would take
effect immediately. Swine and swine
products would not be allowed
importation from the region unless they
are accompanied by certification by an
official of the competent veterinary
authority of the EU–15 Member State
that the prohibitions set forth in this
proposed rule regarding restricted zones
(discussed below) have been met.
In the case of an outbreak of CSF in
EU domestic swine, the importation
prohibitions would remain in effect for
6 months following the depopulation of
swine and the cleaning and disinfection
of the last infected premises in the
restricted zone, even if the competent
veterinary authority of the EU–15
Member State removes its designation of
the area as a restricted zone before 6
months have elapsed. In the case of a
restricted zone established because of
the detection of CSF in wild boar, the
importation prohibitions would remain
in place until the competent veterinary
authority of the EU–15 Member State
removes its designation of the area as a
restricted zone. (The issue of wild boar
is discussed further in this document
under the heading ‘‘Wild Boar.’’) The
lifting of the prohibitions on imports
into the United States from a restricted
zone would take effect at the times
described above. No action by APHIS
would be required. However, APHIS
would reserve the right to make site
visits and review documentation related
to the outbreak and eradication
activities. In considering the CSF risk in
the EU–15, we evaluated both the ability
of officials in that region to ensure that
such restricted zones would be
effectively established and maintained
and the ability of the officials to ensure
that prohibitions on the importation
into the United States of swine and
swine products from the restricted
zones would be effectively enforced.
In §§ 94.0 and 98.30, we would define
restricted zone for classical swine fever
to mean an area, delineated by the
relevant competent veterinary
authorities of the region in which the
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area is located, that surrounds and
includes the location of an outbreak of
CSF in domestic swine or detection of
the disease in wild boar, and from
which the movement of domestic swine
is prohibited. We are not proposing to
specify how far from an outbreak a
restricted zone must extend because
factors such as geographic boundaries
could influence the necessary distance.
However, we did evaluate the policies
of the EC for establishing restricted
zones when considering whether to
consider the EU–15 as a region of lowrisk for CSF. This is discussed in more
detail below under ‘‘EU Animal Health
Controls.’’
We believe this new approach is
warranted for the EU–15 because that
region has demonstrated the capability
to effectively prevent the spread of CSF
from areas where outbreaks occur. Plus,
as a precautionary measure, imports of
swine and swine products from the EU–
15 into the United States will be
restricted to address the recognized
probability of these outbreaks occurring
from time to time.
Because we are proposing to
recognize the EU–15 as a single region
that poses a low risk for CSF, we would
remove from §§ 94.9(a) and 94.10(a) of
the regulations the EU–15 Member
States currently listed as regions in
which CSF is not known to exist. The
EU–15 would be included in proposed
§§ 94.9(b) and 94.10(b) as a single region
of low-risk for CSF.
Basis for Consideration of the EU–15 as
a Region of Low-Risk for CSF
We believe that consideration of the
EU–15 as a single low-risk region for
CSF is warranted based on the risk
analyses described above, upon which
we based on our April 2003 final rule,
and on our knowledge of the veterinary
infrastructure and legislation in the EU.
These considerations are discussed in
detail in an APHIS document titled
‘‘APHIS Risk Considerations on
Importation of Classical Swine Fever
(CSF) Virus in Breeding Swine, Swine
Semen, and Fresh Pork from a European
Union Region of Fifteen Member
States.’’ The document can be obtained
by calling or writing to the person listed
in this document under FOR FURTHER
INFORMATION CONTACT. It is also available
on the Internet at https://
www.aphis.usda.gov/vs/ncie/regrequest.html. At the bottom of that Web
site page, click on ‘‘Information
previously submitted by Regions
requesting export approval and
supporting documentation.’’ At the next
screen, click on the triangle beside
‘‘European Union/Not Specified/
Classical Swine Fever,’’ then click on
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the triangle beside ‘‘Response by
APHIS,’’ which will reveal a link to the
document.
The estimates of risk in the analyses
we conducted regarding CSF in the EU–
15 suggest that the EU’s control
mechanisms, combined with the risk
mitigation measures we established in
the April 2003 final rule, are sufficiently
effective to mitigate the risk of
introducing the CSF virus to the United
States via exports of the swine and
swine products that would be eligible
for importation into the United States
under this rule.
The risk estimated in the risk analyses
regarding the EU that we conducted in
1999 and 2000 was based on
quantitative data reflecting the effects of
EU regulations that were in place during
a severe CSF outbreak in 1997 and 1998
that occurred extensively in the
Netherlands and that spread to other EU
Member States. Although the outbreak
was considered the most severe the EU
ever experienced and CSF did spread
during that outbreak, our quantitative
estimates of risk showed that the risk to
the United States of CSF introduction
due to that most severe outbreak was
low. Since that outbreak, the EU has
implemented measures to strengthen its
response to a CSF outbreak. Therefore,
with the continued application of EU
regulations, any risk from future CSF
outbreaks in the EU–15 is expected to
also be low, unless an outbreak occurs
that is more severe than the one in
1997–1998—i.e., that poses a risk
greater than that evaluated in the
analysis. In the event of a more severe
outbreak or any other circumstance the
Administrator considers to pose a risk
(such as evidence of unreported CSF
outbreaks or significant deterioration of
veterinary infrastructure or control in
the region), the APHIS Administrator
would reserve the right to take whatever
action is necessary to ensure that CSF is
not introduced into the United States.
EU Animal Health Controls
In general, our proposed classification
of the EU–15 as a region of low risk for
CSF is based on continued adherence in
the Member States to EU animal health
controls, some of which are described
below, as well as on the measures we
established in our April 2003 final rule.
However, in one way, we believe it is
necessary to require a measure that
exceeds the EU controls. This measure
has to do with the length of time the
prohibition on the importation into the
United States of swine and swine
products from a restricted zone is
maintained. We discuss this measure at
greater length below, under the heading
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‘‘Prohibition of Importations from a
Restricted Zone.’’
Animal health regulations imposed in
the EU are harmonized and binding
upon all Member States. Requirements
include compulsory notification of OIE
List A diseases, including CSF, and
laboratory testing for CSF on all sick
swine if CSF is suspected. Member
States are required to have CSF
contingency plans and, if applicable,
eradication plans for CSF in wild boar
populations.
Swine are moved freely among EU
Member States and within Member
States. Swine born in one Member State
are routinely fattened or slaughtered in
another. Animals moving between
Member States are required to be
accompanied by an official health
certificate issued by an official
veterinarian appointed by the
competent veterinary authority of the
Member State. Prior notification of the
movement is reported electronically
through an electronic network linking
authorities of the EC and Member
States.3
Farm registration is mandatory, and
each holding is assigned a unique
identification number by the competent
veterinary authority of the Member
State. Animal identification is
compulsory. Breeding swine must be
identified with a unique identification
number (either by ear tag or tattoo), and
fattening swine must be identified by
the holding registration number. This
information is maintained by each
Member State.
If CSF is detected anywhere in the
EU, control mechanisms are activated in
accordance with EU legislation. When
CSF is suspected on a swine holding, a
clinical investigation is conducted by
the competent veterinary authority of
the Member State to confirm or rule out
the disease, and an epidemiological
investigation is carried out. Movement
of swine from the holding under
suspicion is prohibited, and biosecurity
measures are implemented to prevent
spread of the disease.
If CSF is confirmed, all swine on the
holding containing infected swine must
be depopulated, and the carcasses must
be disposed of after being treated to
inactivate the CSF virus under official
supervision. Two types of zones are
3 TRACES (Trade Control and Export System) is
replacing ANIMO by the end of 2004 as the
computerized system mandated by EU law to track
animal and animal product movement between
Member States, as well as to track imports from
non-EU countries into the EU. Data are entered by
local veterinary authorities in each Member State
and are shared over a network with the rest of the
EU. The system is administered by a private
contractor under the oversight of the EC and the EU
Court of Auditors.
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established around an outbreak of CSF
in EU domestic swine—‘‘protection
zones’’ and ‘‘surveillance zones.’’ The
protection zone extends at least 3
kilometers from the outbreak. The
surveillance zone extends at least 10
kilometers from the outbreak. For the
purpose of our regulations, we would
consider the combination of an EU
protection zone and surveillance zone to
constitute a restricted zone. When
establishing zones, the competent
veterinary authority of the Member State
is required by EU legislation to take into
account the following:
• The results of the epidemiological
investigation;
• The geographical situation,
particularly natural or artificial
boundaries;
• The location and proximity of
holdings;
• Patterns of movements and trade in
swine and the availability of
slaughterhouses;
• The facilities and personnel
available to control any movement of
swine within the zones, in particular if
the swine to be killed need to be moved
away from their holding of origin.
Veterinary authorities are required to
take all necessary measures, including
posting signs and alerting the media, to
inform the public of the imposed
restrictions and must use appropriate
measures to enforce the restrictions.
Veterinary authorities of Member States
collaborate in establishing zones that
overlap their borders.
In accordance with EU regulations,
premises located within the protection
zone are prohibited by the Member State
from moving swine out of that zone for
at least 30 days following the
depopulation of swine and the cleaning
and disinfection of the last premises in
the zone infected with CSF. Premises
within the surveillance zone are
prohibited by the Member State from
moving swine out of that zone for at
least 20 days following the
depopulation of swine and the cleaning
and disinfection of the last premises in
the protected zone infected with CSF. A
census is conducted of all swine in both
the protection and surveillance zones.
Clinical examinations are conducted of
all swine within the protection zone.
An epidemiological inquiry is made
into the origin of the virus in the
infected swine, and contacts are
identified for traceback and
traceforward investigations. Isolates of
the virus are genetically typed by the EU
Reference Laboratory in Hanover,
Germany.
Under official supervision of the
competent veterinary authority of the
Member State, meat of swine
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slaughtered during the period between
the probable introduction of disease and
the implementation of control measures
is traced and processed in such a way
as to destroy or inactivate the CSF virus.
Likewise, swine genetic products
collected during this time are traced and
destroyed under official supervision in
such a way as to avoid the risk of spread
of the CSF virus.
After the depopulation of swine, the
buildings, equipment, vehicles, and
other articles that may have been
contaminated with the CSF virus must
be cleaned and disinfected under
official supervision using approved
disinfectants.
Swine may not be reintroduced onto
a holding that contained infected swine
until at least 30 days after the required
cleaning and disinfection. Any swine
reintroduced onto the holding must be
monitored to make sure that none
develop antibodies to CSF.
The EU does not vaccinate domestic
swine for CSF. However, with EC
approval, emergency vaccination may
be used in cases where CSF has been
confirmed and epidemiological data
suggest that the disease threatens to
spread.
Whenever CSF is detected in a wild
boar, the competent veterinary authority
of the Member State, in consultation
with an expert panel of veterinarians,
hunters, wildlife biologists, and
epidemiologists, defines the infected
area, implements appropriate measures
to reduce the spread of the disease,
develops and submits for EC approval
an eradication plan, and audit the
effectiveness of measures adopted to
eradicate CSF from the infected area.
These measures require that all holdings
of domestic swine in the infected area
be placed under official surveillance, an
official census of swine be conducted,
swine movement be restricted,
biosecurity measures be implemented,
and testing for CSF be conducted on all
sick or dead swine. Further, all wild
boar shot or found dead must be
examined and tested for CSF by an
official veterinarian designated by the
competent veterinary authority of the
Member State. In addition, the measures
taken may include suspension of
hunting and a ban on feeding wild boar.
The veterinary authority must also
ensure that the CSF isolate is genetically
typed. Adjacent Member States
collaborate in establishing control
measures in cases where the infected
wild boar are found close to common
borders.
As part of an approved eradication
plan, emergency vaccination of wild
boar may be conducted in situations
where CSF has been confirmed and
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17933
epidemiological data suggest that the
disease threatens to spread. The
vaccination area must be part of the
defined infected area, and appropriate
measures must be taken to prevent
spread of the vaccine virus to domestic
swine. Currently, there is an ongoing
emergency vaccination program for wild
boar in infected areas within Germany
and Luxembourg.
Requirement in Addition to EU Controls
As we stated above, we believe it is
necessary to require a CSF control
measure in the EU–15 that exceeds EU
controls and the conditions imposed by
our April 2003 final rule. This measure
is the length of time the prohibitions on
the exportation of swine and swine
products to the United States are
maintained. We discuss this measure
below.
Prohibition of Importations From a
Restricted Zone
Current EU regulations allow CSF
restrictions in a protection zone (that
area extending at least 3 kilometers from
an infected holding of domestic swine)
to be removed 30 days after completion
of preliminary cleaning and disinfection
measures on the infected holding.
Restrictions in a surveillance zone must
stay in place at least 20 days after such
cleaning and disinfection. Restrictions
are removed only after clinical
examinations and serology indicate that
any swine remaining in the area are free
of CSF. Presumably, after restrictions
are released, swine from the area could
be moved throughout the EU.
We are concerned by observations of
recurrence of CSF in certain areas
shortly after such restrictions have been
removed by the EU and swine
movement from the areas has
commenced. For example, in December
2001, an outbreak was confirmed in
Osoma, Spain, 22 days after release of
movement restrictions by the EU. In
another case, an outbreak in
Luxembourg in August 2002 was
epidemiologically linked to an outbreak
that occurred in June 2002, and
occurred 27 days after release of
movement restrictions by the EU.
During the 1997–1998 epidemic,
veterinary authorities in the EU usually
found it necessary to maintain
movement restrictions for more than 30
days following an outbreak. These
observations suggest that restricting
movement for only 30 days may be
insufficient to ensure that the region
remains unaffected.
Further, as discussed below, we
believe that OIE standards support
restriction of movement for more than
30 days. As discussed above, we are
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proposing to consider the EU–15 as a
region of low risk for CSF, rather than
as a region in which CSF is not known
to exist. The OIE standard that would be
relevant to such a region is the standard
for a country or zone free of CSF in
domestic swine but with infection in the
wild swine population.4 In such
situations, OIE recommends that, where
a stamping out policy without
vaccination has been implemented for
CSF control, recognition of the region as
CSF-free may be acquired 6 months after
the last outbreak in domestic swine.
We are in agreement with the OIE
recommendation that restrictions on the
movement of swine and swine products
from a CSF quarantined area be
maintained for 6 months, and consider
it consistent with our proposed
consideration of the EU–15 as a region
that poses a low risk of CSF. Further,
maintenance of such restrictions for 6
months is consistent with our stated
intent in our December 2000 risk
analysis to accept exports only from
regions that have not experienced a CSF
outbreak within the previous 6 months.5
This is why we are proposing to provide
that our prohibition on the importation
of swine and swine products from a
restricted zone established because of an
outbreak of CSF in domestic swine
remain in place for at least 6 months
following the depopulation of swine
and the cleaning and disinfection of the
last infected premises in the zone. As
noted above, the prohibition of the
importation of swine and swine
products from a restricted zone
established because of the detection of
CSF in wild boar would remain in place
until the restricted zone status of the
area is removed by the competent
veterinary authority of the EU–15
Member State.
Wild Boar
Under our current regulations, we do
not remove a region from the lists in
§§ 94.9(a) and 94.10(a) of regions
considered free of CSF if the disease is
detected in wild boar in the region but
not in domestic swine. This approach is
consistent with APHIS domestic
regulations, which do not regulate wild
boar in the United States for swine
diseases. However, under this proposed
rule, we would prohibit importations of
swine and swine products from areas in
the EU–15 placed under quarantine by
the competent veterinary authority of an
EU–15 Member State because of the
detection of CSF in wild boar, even if
4 OIE, Terrestrial Animal Health Code-2003, Part
2, Chapter 2.1.13.
5 Risk Analysis for Importation of Classical Swine
Fever Virus in Swine and Swine Products from the
European Union—December 2000.
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CSF has not been detected in domestic
swine in the area. Although the
estimates of CSF risk from the region
identified in our 1999 and 2000 risk
analyses were based on data related
only to outbreaks and control measures
in EU domestic swine (i.e., data from
wild boar outbreaks were not included),
we recognize that EU control measures
implemented in response to outbreaks
in wild boar had a mitigating effect on
the spread of CSF in domestic swine.
Therefore, we believe that EU control
measures for CSF in wild boar are a
critical component of the overall EU
controls for CSF. Data indicate that wild
boar continue to be a potential source of
infection in domestic swine. For
example, infected wild boar are the
suspected source of virus linked to an
August 2003 outbreak in Luxembourg,
an April 2002 outbreak in France, and
multiple outbreaks in Germany. The EU
recognizes the risk to its domestic swine
population because of the endemic CSF
infection in wild boar and has
implemented eradication plans and
contingency measures to deal with this
problem. To protect domestic swine
herds throughout the region, the EC has
placed restrictions on movement of
domestic swine from infected wild boar
areas. It is likely that the EU restrictions
on regions containing infected wild boar
contribute significantly to the
effectiveness of EU control measures.
Certificate for Swine
Section 93.505 of the regulations
requires that, except for swine from
Canada, all swine intended for
importation into the United States be
accompanied by official certification
regarding the health status of the swine
and the disease status of the region of
origin. Paragraph (a) of § 93.505 requires
that the certificate accompanying the
swine show that the entire region of
origin of the swine is free of CSF. In
accordance with our proposed action to
allow the importation of breeding swine
from the EU–15, we are proposing to
change the language in § 93.505
accordingly, to allow for the importation
of live swine from the EU–15.
Application of this Approach to Other
Regions
Section 92.2 of the regulations defines
the type of information that must be
included with the request of a country
or countries to APHIS for recognition of
the animal health status of a region.
Evaluation of this information would
constitute the first step in consideration
of a new regulatory approach for the
region. As part of its consideration,
APHIS would determine whether it
might be appropriate to revise its
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approach dealing with outbreaks in the
region that made the request. The
results of these considerations will be
reflected in regulatory changes made
through rulemaking. Aspects of the
rulemaking process are discussed in
§ 92.2.
Authorized Inspectors
Currently, there is a requirement in
§ 94.24(c) that certificates required
under § 94.24 be presented by the
importer of swine and swine products to
the appropriate Customs and Border
Protection officer at the port of arrival.
We are proposing to require instead that
the certificates be presented to an
authorized inspector, which is defined
in § 94.0 as any individual authorized
by the Administrator of APHIS or the
Commissioner of Customs and Border
Protection, Department of Homeland
Security, to enforce the regulations. This
change would reflect the fact that, for
some imports, it is an APHIS employee
who accepts the certificate at the port of
arrival.
Executive Order 12866 and Regulatory
Flexibility Act
This proposed rule has been reviewed
under Executive Order 12866. The rule
has been determined to be significant
for the purposes of Executive Order
12866 and, therefore, has been reviewed
by the Office of Management and
Budget.
Under the Animal Health Protection
Act (7 U.S.C. 8301 et seq.) the Secretary
of Agriculture is authorized to
promulgate regulations to prevent the
introduction into the United States or
dissemination of any pest or disease of
livestock. Under this authority, APHIS
is proposing to establish provisions for
imports of swine and swine products
from the EU–15 under conditions we
believe will guard against the
introduction of CSF into the United
States from that region.
Below is the economic analysis for the
changes proposed in this document. The
economic analysis provides a costbenefit analysis as required by
Executive Order 12866 and an analysis
of the potential economic effects on
small entities as required by the
Regulatory Flexibility Act.
We do not have enough data for a
comprehensive analysis of the economic
effects of this proposed rule on small
entities. Therefore, in accordance with 5
U.S.C. 603, we have performed an initial
regulatory flexibility analysis for this
proposed rule. We are inviting
comments about this proposed rule as it
relates to small entities. In particular,
we are interested in determining the
number and kind of small entities who
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may incur benefits or costs from
implementation of this proposed rule
and the economic impact of those
benefits or costs.
CSF is a highly contagious and fatal
disease of swine. It was eradicated from
the United States in 1976 after a 16-year
effort, at a cost to USDA and individual
States of about $140 million ($455
million in 2003 dollars). The potential
for reintroduction of CSF into the
United States remains a major concern,
not only because of production losses
and eradication costs, but also because
of the adverse effects reintroduction
would have on U.S. swine and pork
exports.
APHIS determines, based on disease
risk evaluations, whether animals and
animal products may be exported from
foreign regions to the United States. If
a region recognized by APHIS as free of
a specific animal disease experiences an
outbreak, generally an interim rule is
issued prohibiting or restricting
potentially infected imports. Once the
outbreak has been eliminated, and a
period of time has elapsed sufficient to
allow the animal disease situation in the
region to stabilize, the region’s previous
disease-free status may be restored.
APHIS personnel conduct a site visit
and reevaluate the risk by conducting a
risk analysis. If, based on the analysis,
APHIS believes it is appropriate to once
again consider the region free of the
disease, APHIS publishes a notice in the
Federal Register soliciting public
comments on the analysis. Any
comments received are reviewed and
each issue raised by commenters is
considered. If, after review of the
comments, APHIS continues to consider
it appropriate to once again recognize
the region free of the disease, a final rule
is published in the Federal Register
giving notice of such recognition.
We believe this proposed rule would
enable APHIS to respond more quickly
to changes in CSF conditions within the
EU–15, while maintaining the Agency’s
sanitary standards. The proposed rule
would change the procedure by which
imports of swine, pork and pork
products, and swine semen would be
allowed to resume following the
elimination of a CSF outbreak in the
EU–15. Separate rulemaking would no
longer be required each time an area
within the region experiences a CSF
outbreak and the disease is
subsequently eliminated. Rather, APHIS
would recognize quarantine decisions
made by the competent veterinary
authority of an EU–15 Member State
and prohibit the importation of swine
and swine products from restricted
zones in the EU–15 established by the
competent veterinary authority of an
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EU–15 Member State. As an additional
safeguard, imports of swine, fresh pork
and pork products, and swine semen
into the United States from the
restricted zone would be prohibited for
a period of 6 months following the
depopulation of swine and the cleaning
and disinfection of the last infected
premises in the zone. Restrictions and
prohibitions we would establish
because of the detection of CSF in wild
boar would remain in place until the
restricted zone status of the area is
removed by a competent veterinary
authority of the EU–15 Member State.
An alternative to the proposed rule
would be to not change the
regulations—i.e., to continue to initiate
rulemaking whenever the CSF situation
within the EU–15 changes. Continuing
with the current procedures would not
achieve the Agency objective of
improving the Agency’s responsiveness
to CSF situation changes while
maintaining adequate disease
prevention measures. A second
alternative would be to consider the
EU–15 as a single region of low risk for
CSF, but not require that at least 6
months elapse after eradication of a
disease outbreak in the region before the
importation of swine and swine
products into the United States could
resume. This alternative would forfeit
the additional sanitary assurance that
the 6-month period is intended to
provide to the U.S. swine industry that
the reestablished imports would be CSFfree. We believe that this proposed rule
would be preferable in allowing
resumption of imports in a timelier
manner, while ensuring that sanitary
standards are maintained. As noted
above, we invite public comment on
this proposed rule, including comment
on how the proposed rule could be
modified to reduce expected costs or
burdens for small entities consistent
with its objectives. Any comment
suggesting changes to the proposed
criteria should be supported by an
explanation of why the changes should
be made.
Expected Effects of the Proposed Rule
This proposed rule could affect U.S.
imports of swine, pork and pork
products, and swine semen from the
EU–15 in several ways. One of the
effects would be potential additional
restrictions on the importation of swine
semen from certain EU–15 Member
States. Additionally, the regulatory
process used to establish import
restrictions for areas affected by CSF,
and to remove those restrictions when
the disease is eliminated, would be
simplified and made timelier. We
believe the proposed rule would also
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result in more efficient use of APHIS
resources. These areas of potential
effects are discussed in turn.
Change in Swine Semen Requirements
The EU–15 consists of the following
Member States: Austria, Belgium,
Denmark, Finland, France, Germany,
Greece, Italy, Luxembourg, the
Netherlands, Portugal, the Republic of
Ireland, Spain, Sweden, and the United
Kingdom. APHIS considered five of the
Member States—Denmark, Finland, the
Republic of Ireland, Sweden, and the
United Kingdom—to be free of CSF even
before publication of our April 2003
final rule. In that final rule, we
recognized—with the exception of
specified regions in Germany and
Italy—the countries of Austria, Belgium,
Germany, Greece, Italy, the Netherlands,
and Portugal as a single region in which
CSF is not known to exist. That final
rule also set forth conditions under
which breeding swine, pork and pork
products, and swine semen could be
imported into the United States from
that region.
The remaining three Member StatesFrance, Luxembourg, and Spain-as well
as specified regions in Germany and in
Italy, were not included in the region
recognized by the final rule because of
outbreaks of CSF either before or after
publication of the June 1999 proposed
rule on which the April 2003 final rule
was based. However, as discussed
above, we published a final rule in the
Federal Register in April 2004 that
recognized France and Spain as part of
the CSF-free region we had established
in our April 2003 final rule.
This proposed rule would consider
the EU–15 to be a single region of lowrisk for CSF. Therefore, that region
would include the seven Member States
we recognized in whole or in part as
CSF-free in the April 2003 final rule
(Austria, Belgium, Germany, Greece,
Italy, the Netherlands, and Portugal), the
five Member States we already
considered CSF-free before the April
2003 final rule (Denmark, Finland, the
Republic of Ireland, Sweden, and the
United Kingdom), the two Member
States we recognized as CSF-free in our
April 2004 final rule (France and
Spain), and Luxembourg. Under the
provisions of this proposed rule, each of
the 15 Member States would be subject
to the import conditions set forth in the
April 2003 final rule and to the
restrictions added in this document
concerning waiting periods before
release of restrictions on zones where
outbreaks have occurred. In considering
the effects of these changes, the key
questions are: (1) In what ways do the
current import requirements for
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Denmark, Finland, the Republic of
Ireland, Sweden, and the United
Kingdom differ from the import
requirements set forth in this proposed
rule; and (2) what effects would result
for those five Member States due to the
changes in requirements for export to
the United States?
This proposed rule prescribes
conditions for the importation of
breeding swine, swine semen, and pork
and pork products from areas classified
as low risk for CSF. Movement
restrictions require that there be no
commingling of commodities intended
for export to the United States (or of the
donor boars of swine semen intended
for export to the United States) with like
commodities from areas where CSF is
known to exist. Movement of
commodities intended for export to the
United States through areas where CSF
is known to exist is permitted only by
sealed means of conveyance. Sanitary
certification that these provisions have
been met is required.
Denmark, Finland, the Republic of
Ireland, Sweden, and the United
Kingdom are already complying with
the proposed conditions for pork, pork
products, and breeding swine, and, in
fact, were meeting these conditions
before our April 2003 final rule.
However, with respect to swine semen,
the proposal would require that before
the semen is exported to the United
States, the donor boar must be held at
the semen collection center for at least
40 days following semen collection, to
ensure that the boar does not exhibit
any clinical signs of CSF. This would be
a new risk mitigation measure for swine
semen exported to the United States
from these five Member States.
Three of the five Member States,
Denmark, the Republic of Ireland, and
the United Kingdom, have histories of
swine semen exports to the United
States. From 1994 through 2002, the
United States imported an average of
2,474 straws of swine semen annually.
The average yearly share of U.S. swine
semen imports supplied by the three
Member States over the 9-year period
was about 26 percent. The United
Kingdom was the major source among
the three Member States, supplying all
of the three Member States’ swine
semen exports to the United States in 5
of the 9 years.
Reportedly, donor boars are largely
resident at swine collection centers, so
costs associated with the animals’
maintenance would be affected little by
the 40-day holding period. A potential
issue is whether storage for 40 days
before exportation would affect the
quality of the collected semen and
therefore affect import demand. APHIS
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welcomes information on this issue that
may help in evaluating the effect on
swine semen importers.
More Timely Reestablishment of CSFFree Status
The proposed procedure for
reestablishing CSF-free status for an area
that has been under quarantine is
expected to require less time than
current procedures, notwithstanding the
6-month restriction following the last
case of CSF and completion of
disinfection measures. More timely
recognition of an area’s CSF-free status
would allow imports of swine and
swine products from the area to resume
sooner than at present. The effect of this
procedural change would depend on the
difference in time required by the two
regulatory approaches, and the
additional swine, swine meat, and
swine genetics that would be imported
because of more timely recognition of an
area’s reestablished CSF-free status.
APHIS published a final rule on May
4, 2004 (69 FR 25817–25820, Docket No.
02–001–2) that codifies the procedures
APHIS follows when a region free of a
particular disease has an outbreak and
APHIS responds to that outbreak by
publishing an interim rule prohibiting
or restricting imports from that region.
APHIS will reassess the disease
situation in that region, and, before
taking any action to relieve or finalize
prohibitions or restrictions imposed by
the interim rule, will make information
regarding its reassessment of the
region’s disease status available to the
public for comment. Based on that
reassessment, including comments
received regarding the reassessment
information, APHIS will either publish
a final rule reinstating the disease-free
status of the area, or a portion of the
area covered by the interim rule;
publish an affirmation of the interim
rule that imposed prohibitions or
restrictions on imports of animals and
animal products from that area; or
publish another document for comment.
Under procedures in place previously,
APHIS affirmed the initial interim rule,
and then conducted new notice-andcomment rulemaking (proposed rule,
comment period, final rule) in order to
restore a region’s disease-free status.
The new procedures the Agency
codified allow for more timely
reinstatement of an area’s disease-free
status, while protecting the U.S. swine
sector. We believe the rule we are now
proposing would further improve the
timeliness of APHIS’s recognition of
changes in CSF status in the EU–15.
As noted in the economic analysis for
the May 2004 final rule, quantities of
animals and animal products imported
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by the United States are relatively small
in comparison to the total quantities
available domestically. In addition, the
majority of the imports come from a
small fraction of the world’s disease-free
regions. Also, it is very difficult to
quantify the potential economic effects
of more timely recognition of changes in
CSF status. We believe the major benefit
of this proposed rule would be
improved trade relations between the
United States and the EU. Less than 6
percent of domestically available swine
(U.S. production plus imports minus
exports) and less than 3 percent of
domestically available pork are
imported. The majority of swine imports
come from one country, Canada, and the
majority of swine product imports come
from two, Canada and Denmark. We
cannot predict the number of swine or
quantity of swine products that this
proposed rule would affect, but they are
unlikely to be significant. One or more
of the areas not yet recognized by the
United States as free of CSFLuxembourg and parts of Germany and
Italy—may be among the first to benefit
from this rule.
More Efficient Use of APHIS Resources
A third area of impact would be the
effect of the proposed rule on APHIS
operations. Just as the proposed rule
could enable imports of swine, swine
meat, and swine genetics to resume
more quickly from areas that experience
and then eradicate outbreaks of CSF, so
too would it result in fewer site visits,
risk analyses, Federal Register
publications and other rulemaking tasks
for APHIS. Resources that are devoted to
tasks currently required for changing the
CSF status of areas in the European
Union would become available for other
uses.
As with the impact on imports,
expected gains in the efficient use of
Agency resources cannot be quantified.
They would be realized in terms of the
additional time APHIS staff would have
for other tasks, and would depend on
the frequency with which CSF
quarantines and CSF-free status
reinstatements occur within the
European Union.
We believe that the benefits that
would accrue from this rule—i.e.,
improved trade relations with the EU
through more timely recognition of
changes in CSF status, as well as
increased efficiency in use of APHIS
resources—would outweigh any
increased costs to importers of swine
semen from certain EU Member States
that would result from an extended
waiting period between when the semen
is collected and when shipment may
occur.
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Federal Register / Vol. 70, No. 67 / Friday, April 8, 2005 / Proposed Rules
Effects on Small Entities
As a part of the rulemaking process,
APHIS evaluates whether proposed
regulations would likely have a
significant economic impact on a
substantial number of small entities.
U.S. entities that could be affected by
the proposed rule would be swine and
pork producers and swine product
wholesalers.
The size of the potentially affected
entities is unknown. However, it is
reasonable to assume that most are
small in size under the U.S. Small
Business Administration’s (SBA)
standards. The SBA defines small hog
and pig farms as those earning not more
than $750,000 in annual receipts.
National Agricultural Statistics Service
data on hog farm inventories include
farm size categories, including the
number of farms with more than 1,000
head. Only those swine operations with
inventories well in excess of 3,000
animals would likely earn more than
$750,000 in yearly sales. About 85
percent of 78,895 hog and pig farms in
2002 held inventories of fewer than
1,000 head. The number of operations
with fewer than 3,000 is very likely to
be much higher than 85 percent of all
hog and pig farms. An earlier Census of
Agriculture (1997) had more detail on
farm size and showed that over 95
percent of U.S. swine operations held
inventories of less than 2,000 head.
Clearly, most swine and pork producers
are small entities.
Likewise, swine product wholesalers
are also mainly small entities. The SBA
small entity definition for these
businesses is not more than 100
employees. We do not know the size
distribution of meat wholesalers, but the
2002 Economic Census indicates that
the 2,889 establishments in that
category had an average of 15
employees.
We invite comment from the public
that would clarify the number of swine
operations and swine product
wholesalers that are small entities that
would be affected by this rule.
Although the industries that would be
affected by the proposed rule are largely
composed of small entities, the effects
are not expected to be significant.
Imports of swine semen from Denmark,
Finland, the Republic of Ireland,
Sweden, and the United Kingdom may
be affected if the 40-day holding period
for donor boars before the semen may be
imported influences U.S. demand.
However, even if there is an effect, most
swine semen that is imported comes
from other countries—Canada, in
particular. The more timely
reestablishment of an area’s CSF-free
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status may affect individual entities that
have arranged for imports from that
area, but, as described, such effects are
expected to be minor.
This proposed rule contains various
recordkeeping and reporting
requirements. These requirements are
described in this document under the
heading ‘‘Paperwork Reduction Act.’’
Executive Order 12988
This proposed rule has been reviewed
under Executive Order 12988, Civil
Justice Reform. If this proposed rule is
adopted: (1) All State and local laws and
regulations that are inconsistent with
this rule will be preempted; (2) no
retroactive effect will be given to this
rule; and (3) administrative proceedings
will not be required before parties may
file suit in court challenging this rule.
Paperwork Reduction Act
In accordance with section 3507(d) of
the Paperwork Reduction Act of 1995
(44 U.S.C. 3501 et seq.), the information
collection or recordkeeping
requirements included in this proposed
rule have been submitted for approval to
the Office of Management and Budget
(OMB). Please send written comments
to the Office of Information and
Regulatory Affairs, OMB, Attention:
Desk Officer for APHIS, Washington, DC
20503. Please state that your comments
refer to Docket No. 02–046–1. Please
send a copy of your comments to: (1)
Docket No. 02–046–1, Regulatory
Analysis and Development, PPD,
APHIS, Station 3C71, 4700 River Road
Unit 118, Riverdale, MD 20737–1238,
and (2) Clearance Officer, OCIO, USDA,
room 404-W, 14th Street and
Independence Avenue SW.,
Washington, DC 20250. A comment to
OMB is best assured of having its full
effect if OMB receives it within 30 days
of publication of this proposed rule.
Under this proposed rule, we would
apply a uniform set of importation
requirements related to CSF to the EU–
15 and prohibit for a specified period of
time the importation of live swine and
swine products from any area in the
EU–15 that is identified by the
competent veterinary authority of an
EU–15 Member State as a restricted
zone.
These importation requirements
would necessitate the use of additional
certification statements in connection
with the importation of live swine, pork
and pork products, and swine semen
imported into the United Sates from the
EU–15.
We are soliciting comments from the
public (as well as affected agencies)
concerning our proposed information
collection and recordkeeping
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17937
requirements. These comments will
help us:
(1) Evaluate whether the proposed
information collection is necessary for
the proper performance of our agency’s
functions, including whether the
information will have practical utility;
(2) Evaluate the accuracy of our
estimate of the burden of the proposed
information collection, including the
validity of the methodology and
assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and
(4) Minimize the burden of the
information collection on those who are
to respond (such as through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology; e.g., permitting
electronic submission of responses).
Estimate of burden: Public reporting
burden for this collection of information
is estimated to average 1 hour per
response.
Respondents: Federal animal health
authorities in the European Union who
will complete certificates to export
swine, pork and pork products, and
swine semen to the United States.
Estimated annual number of
respondents: 115.
Estimated annual number of
responses per respondent: 8.695.
Estimated annual number of
responses: 1,000.
Estimated total annual burden on
respondents: 1,000 hours. (Due to
averaging, the total annual burden hours
may not equal the product of the annual
number of responses multiplied by the
reporting burden per response.)
Copies of this information collection
can be obtained from Mrs. Celeste
Sickles, APHIS’ Information Collection
Coordinator, at (301) 734-7477.
Government Paperwork Elimination
Act Compliance
The Animal and Plant Health
Inspection Service is committed to
compliance with the Government
Paperwork Elimination Act (GPEA),
which requires Government agencies in
general to provide the public the option
of submitting information or transacting
business electronically to the maximum
extent possible. For information
pertinent to GPEA compliance related to
this proposed rule, please contact Mrs.
Celeste Sickles, APHIS’ Information
Collection Coordinator, at (301) 734–
7477.
Accordingly, we are proposing to
amend 9 CFR parts 93, 94, and 98 as
follows:
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Federal Register / Vol. 70, No. 67 / Friday, April 8, 2005 / Proposed Rules
List of Subjects
9 CFR Part 93
Animal diseases, Imports, Livestock,
Poultry and poultry products,
Quarantine, Reporting and
recordkeeping requirements.
9 CFR Part 94
Animal diseases, Imports, Livestock,
Meat and meat products, Milk, Poultry
and poultry products, Reporting and
recordkeeping requirements.
9 CFR Part 98
Animal diseases, Imports.
region of origin is free of classical swine
fever.
*
*
*
*
*
PART 94—RINDERPEST, FOOT-ANDMOUTH DISEASE, FOWL PEST (FOWL
PLAGUE), EXOTIC NEWCASTLE
DISEASE, AFRICAN SWINE FEVER,
CLASSICAL SWINE FEVER, AND
BOVINE SPONGIFORM
ENCEPHALOPATHY: PROHIBITED
AND RESTRICTED IMPORTATIONS
4. The authority citation for part 94
would continue to read as follows:
Authority: 7 U.S.C. 450, 7701–7772, and
8301–8317; 21 U.S.C. 136 and 136a; 31
U.S.C. 9701; 7 CFR 2.22, 2.80, and 371.4.
PART 93—IMPORTATION OF CERTAIN
ANIMALS, BIRDS, AND POULTRY,
AND CERTAIN ANIMAL, BIRD, AND
POULTRY PRODUCTS;
REQUIREMENTS FOR MEANS OF
CONVEYANCE AND SHIPPING
CONTAINERS
5. In § 94.0, definitions of European
Union–15 (EU–15) and restricted zone
for classical swine fever would be
added, in alphabetical order, to read as
follows:
1. The authority citation for part 93
would continue to read as follows:
*
Authority: 7 U.S.C. 1622 and 8301–8317;
21 U.S.C. 136 and 136a; 31 U.S.C. 9701; 7
CFR 2.22, 2.80, and 371.4.
2. In § 93.500, a new definition of
European Union–15 (EU–15) would be
added, in alphabetical order, to read as
follows:
§ 93.500
Definitions.
*
*
*
*
*
European Union–15 (EU–15). The
organization of Member States
consisting of Austria, Belgium,
Denmark, Finland, France, Germany,
Greece, Italy, Luxembourg, the
Netherlands, Portugal, Republic of
Ireland, Spain, Sweden, and the United
Kingdom (England, Scotland, Wales, the
Isle of Man, and Northern Ireland).
*
*
*
*
*
3. In § 93.505, paragraph (a), the
second sentence would be removed and
two sentences would be added in their
place to read as follows:
§ 93.505
Certificate for swine.
(a) * * * For domestic swine, the
certificate shall also show that the entire
region of origin is free of African swine
fever and swine vesicular disease and
that, for 60 days immediately preceding
the time of movement from the premises
of origin, no swine erysipelas or swine
plague has existed on such premises or
on adjoining premises. Additionally,
except for the region consisting of the
EU–15 for the purposes of classical
swine fever, for which alternative
certification is required under
§ 94.24(b)(4), for domestic swine the
certificate shall show that the entire
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§ 94.0
Definitions.
*
*
*
*
European Union–15 (EU–15). The
organization of Member States
consisting of Austria, Belgium,
Denmark, Finland, France, Germany,
Greece, Italy, Luxembourg, the
Netherlands, Portugal, Republic of
Ireland, Spain, Sweden, and the United
Kingdom (England, Scotland, Wales, the
Isle of Man, and Northern Ireland).
*
*
*
*
*
Restricted zone for classical swine
fever. An area, delineated by the
relevant competent veterinary
authorities of the region in which the
area is located, that surrounds and
includes the location of an outbreak of
classical swine fever in domestic swine
or detection of the disease in wild boar,
and from which the movement of
domestic swine is prohibited.
*
*
*
*
*
6. Section 94.9 would be amended as
follows:
a. Paragraph (a) and footnote 10
would be revised to read as set forth
below.
b. Paragraphs (b) and (c) would be
redesignated as paragraphs (c) and (d),
respectively.
c. A new paragraph (b) would be
added to read as set forth below.
d. The introductory text of newly
designated paragraph (c) would be
revised to read as set forth below.
e. In newly redesignated paragraph
(c)(1)(iii)(C)(2), the words ‘‘paragraph
(b)’’ would be removed each time they
occur and the words ‘‘paragraph (c)’’
would be added in their place.
f. In newly redesignated paragraph
(c)(2), the words ‘‘paragraph (b)’’ would
be removed and the words ‘‘paragraph
(c)’’ would be added in their place.
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g. In newly redesignated paragraph
(c)(3), the words ‘‘paragraph (b)’’ would
be removed each time they occur and
the words ‘‘paragraph (c)’’ would be
added in their place.
h. In newly redesignated paragraph
(d), the words ‘‘paragraph (b)’’ would be
removed and the words ‘‘paragraph (c)’’
would be added in their place.
§ 94.9 Pork and pork products from
regions where classical swine fever exists.
(a) Classical swine fever is known to
exist in all regions of the world except
Australia; Canada; Chile; Fiji; Iceland;
the Mexican States of Baja California,
Baja California Sur, Chihuahua, and
Sinaloa; New Zealand; Norway; and
Trust Territory of the Pacific Islands.10
(b) The EU–15 is a single region of
low-risk for CSF.
(c) Except as provided in § 94.24 for
the EU–15, no fresh pork or pork
product may be imported into the
United States from any region where
classical swine fever is known to exist
unless it complies with the following
requirements:
*
*
*
*
*
7. Section 94.10 would be revised to
read as follows:
§ 94.10 Swine from regions where
classical swine fever exists.
(a) Classical swine fever is known to
exist in all regions of the world, except
Australia; Canada; Chile; Fiji; Iceland;
the Mexican States of Baja California,
Baja California Sur, Chihuahua, and
Sinaloa; New Zealand; Norway; and
Trust Territory of the Pacific Islands.
(b) The EU–15 is a single region of
low-risk for CSF.
(c) Except as provided in § 94.24 for
the EU–15, no swine that are moved
from or transit any region where
classical swine fever is known to exist
may be imported into the United States,
except for wild swine imported into the
United States in accordance with
paragraph (d) of this section.
(d) Wild swine may be allowed
importation into the United States by
the Administrator upon request in
specific cases under § 93.501 or § 93.504
(c) of this chapter.
8. Section 94.24 would be revised to
read as follows:
§ 94.24 Restrictions on the importation of
pork, pork products, and swine from the
EU–15.
(a) Pork and pork products. In
addition to meeting all other applicable
provisions of this part, fresh pork and
10 See also other provisions of this part and parts
93, 95, and 96 of this chapter, and part 327 of this
title, for other prohibitions and restrictions upon
the importation of swine and swine products.
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Federal Register / Vol. 70, No. 67 / Friday, April 8, 2005 / Proposed Rules
pork products imported from the EU–15
must meet the following conditions:
(1) The pork and pork products must
not have been commingled with pork or
pork products derived from swine that
have been in any of the following
regions or zones:
(i) Any region when the region was
classified in §§ 94.9(a) and 94.10(a) as
one in which classical swine fever is
known to exist, except for the EU–15;
and
(ii) During the following time periods
in any restricted zone in the EU–15:
(A) In a restricted zone established
because of an outbreak of classical
swine fever in domestic swine, during
the 6 months following depopulation of
the swine in the restricted zone and the
cleaning and disinfection of the last
infected premises in the zone; or
(B) In a restricted zone established
because of the detection of classical
swine fever in wild boar, until the
designation of the zone as a restricted
zone is removed by the competent
veterinary authority of an EU–15
Member State.
(2) The swine from which the pork or
pork products were derived must not
have lived in any region or zone listed
in paragraph (a)(1)(i) or (ii) of this
section, and must not have transited any
such region or zone unless moved
directly through the region or zone in a
sealed means of conveyance with the
seal determined to be intact upon arrival
at the point of destination.
(3) The pork and pork products must
be accompanied by a certificate issued
by an official of the competent
veterinary authority of the EU–15
Member State who is authorized to issue
the foreign meat inspection certificate
required by § 327.4 of this title, stating
that the applicable provisions of
paragraphs (a)(1) and (a)(2) of this
section have been met.19
(b) Live swine. In addition to meeting
all other applicable provisions of this
title, live swine imported from the EU–
15 meet the following conditions:
(1) The swine must be breeding
swine;
(2) The swine must not have lived in
any region or zone listed in paragraph
(a)(1)(i) or (ii) or this section, must not
have transited any such region or zone
unless moved directly through the
region or zone in a sealed means of
conveyance with the seal determined to
be intact upon arrival at the point of
destination, and must never have been
commingled with swine that were in
such a region.
19 The certification required may be placed on the
foreign meat inspection certificate required by
§ 327.4 of this title or may be contained in a
separate document.
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(3) No equipment or materials used in
transporting the swine may have
previously been used for transporting
swine that do not meet the requirements
of this section, unless the equipment
and materials have first been cleaned
and disinfected; and
(4) The swine must be accompanied
by a certificate issued by a salaried
veterinary officer of the competent
veterinary authority of the EU–15
Member State, stating that the
conditions of paragraphs (b)(1) through
(b)(3) of this section have been met.20
(c) The certificates required by
paragraphs (a)(3) and (b)(4) of this
section must be presented by the
importer to an authorized inspector at
the port of arrival, upon arrival of the
swine, pork, or pork products at the
port.
(Approved by the Office of
Management and Budget under control
number 0579–0218)
PART 98—IMPORTATION OF CERTAIN
ANIMAL EMBRYOS AND SEMEN
9. The authority citation for part 98
would continue to read as follows:
Authority: 7 U.S.C. 1622 and 8301–8317;
21 U.S.C. 136 and 136a; 31 U.S.C. 9701; 7
CFR 2.22, 2.80, and 371.4.
10. In § 98.30, definitions of European
Union–15 (EU–15) and restricted zone
for classical swine fever would be
added, in alphabetical order, to read as
follows:
§ 98.30
Definitions.
*
*
*
*
*
European Union–15 (EU–15). The
organization of Member States
consisting of Austria, Belgium,
Denmark, Finland, France, Germany,
Greece, Italy, Luxembourg, the
Netherlands, Portugal, Republic of
Ireland, Spain, Sweden, and the United
Kingdom (England, Scotland, Wales, the
Isle of Man, and Northern Ireland).
*
*
*
*
*
Restricted zone for classical swine
fever. An area, delineated by the
relevant competent veterinary
authorities of the region in which the
area is located, that surrounds and
includes the location of an outbreak of
CSF in domestic swine or detection of
the disease in wild boar, and from
which the movement of domestic swine
is prohibited.
*
*
*
*
*
11. Section 98.38 would be revised to
read as follows:
20 The certification required may be placed on the
certificate required by § 93.505(a) of this chapter or
may be contained in a separate document.
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17939
§ 98.38 Restrictions on the importation of
swine semen from the EU–15.
In addition to meeting all other
applicable provisions of this part, swine
semen imported from the EU–15 must
meet the following conditions:
(a) The semen must come from a
semen collection center approved for
export by the competent veterinary
authority of the EU–15 Member State;
(b) The donor boar must not have
lived in any region or zone listed in
paragraph (b)(1) or (b)(2) of this section,
must not have transited any such region
or zone unless moved directly through
the region or zone in a sealed means of
conveyance with the seal determined to
be intact upon arrival at the point of
destination, and must never have been
commingled with swine that were in
such a region:
(1) Any region when the region was
classified in §§ 94.9(a) and 94.10(a) of
this chapter as one in which classical
swine fever is known to exist, except for
the EU–15; and
(2) During the following time periods
in any restricted zone in the EU–15:
(i) In a restricted zone established
because of an outbreak of classical
swine fever in domestic swine, during
the 6 months following depopulation of
the swine in the restricted zone and the
cleaning and disinfection of the last
infected premises in the zone; or
(ii) In a restricted zone established
because of the detection of classical
swine fever in wild boar, until the
designation of the zone as a restricted
zone is removed by the competent
veterinary authority of the EU–15
Member State.
(c) The donor boar must be held in
isolation for at least 30 days prior to
entering the semen collection center;
(d) No more than 30 days prior to
being held in isolation as required by
paragraph (c) of this section, the donor
boar must be tested with negative
results with a classical swine fever test
approved by the Office International des
Epizooties (World Organisation for
Animal Health);
(e) No equipment or materials used in
transporting the donor boar from the
farm of origin to the semen collection
center may have been used previously
for transporting swine that do not meet
the requirements of this section, unless
such equipment or materials has first
been cleaned and disinfected;
(f) Before the semen is exported to the
United States, the donor boar must be
held at the semen collection center and
observed by the center veterinarian for
at least 40 days following collection of
the semen, and, along with all other
swine at the semen collection center,
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Federal Register / Vol. 70, No. 67 / Friday, April 8, 2005 / Proposed Rules
27 CFR Part 9
• https://www.regulations.gov (Federal
e-rulemaking portal; follow instructions
for submitting comments).
You may view copies of this notice,
the petition, the appropriate maps, and
any comments we receive about this
notice by appointment at the TTB
Library, 1310 G Street, NW.,
Washington, DC 20220. To make an
appointment, call 202–927–2400. You
may also access copies of the notice and
comments online at https://www.ttb.gov/
alcohol/rules/index.htm.
See the Public Participation section of
this notice for specific instructions and
requirements for submitting comments,
and for information on how to request
a public hearing.
FOR FURTHER INFORMATION CONTACT: Rita
Butler, Regulations and Procedures
Division, Alcohol and Tobacco Tax and
Trade Bureau, 1310 G Street NW.,
Washington, DC 20220; telephone 202–
927–8210.
SUPPLEMENTARY INFORMATION:
[Notice No. 39]
Background on Viticultural Areas
RIN 1513–AA95
TTB Authority
Section 105(e) of the Federal Alcohol
Administration Act (the FAA Act, 27
U.S.C. 201 et seq.) requires that alcohol
beverage labels provide the consumer
with adequate information regarding a
product’s identity and prohibits the use
of misleading information on such
labels. The FAA Act also authorizes the
Secretary of the Treasury to issue
regulations to carry out its provisions.
The Alcohol and Tobacco Tax and
Trade Bureau (TTB) administers these
regulations.
Part 4 of the TTB regulations (27 CFR
part 4) allows the establishment of
definitive viticultural areas and the use
of their names as appellations of origin
on wine labels and in wine
advertisements. Part 9 of the TTB
regulations (27 CFR part 9) contains the
list of approved viticultural areas.
exhibit no clinical signs of classical
swine fever; and
(g) The semen must be accompanied
to the United States by a certificate
issued by a salaried veterinary officer of
the EU–15 Member State, stating that
the provisions of paragraphs (a) through
(f) of this section have been met.3
[Approved by the Office of Management and
Budget under control number 0579–0218]
Done in Washington, DC, this 4th day of
April 2005.
Bill Hawks,
Under Secretary for Marketing and Regulatory
Programs.
[FR Doc. 05–7013 Filed 4–7–05; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF THE TREASURY
Alcohol and Tobacco Tax and Trade
Bureau
Proposed Establishment of the
Shawnee Hills Viticultural Area
(2002R–345P)
Alcohol and Tobacco Tax and
Trade Bureau, Treasury.
ACTION: Notice of proposed rulemaking.
AGENCY:
SUMMARY: The Alcohol and Tobacco Tax
and Trade Bureau proposes to establish
the Shawnee Hills viticultural area in
southern Illinois. This proposed
1,268,960-acre viticultural area is
approximately 80 miles long east to
west and approximately 20 miles wide
from north to south. We designate
viticultural areas to allow vintners to
better describe the origin of their wines
and to allow consumers to better
identify wines they may purchase. We
invite comments on this proposed
addition to our regulations.
DATES: We must receive your written
comments on or before June 7, 2005.
ADDRESSES: You may send comments to
any of the following addresses:
• Chief, Regulations and Procedures
Division, Alcohol and Tobacco Tax and
Trade Bureau, Attn: Notice No. 39, P.O.
Box 14412, Washington, DC 20044–
4412.
• 202–927–8525 (facsimile).
• nprm@ttb.gov (e-mail).
• https://www.ttb.gov/alcohol/rules/
index.htm. An online comment form is
posted with this notice on our Web site.
3 The certification required may be placed on the
certificate required under § 98.35(c) or may be
contained in a separate document.
VerDate jul<14>2003
15:28 Apr 07, 2005
Jkt 205001
Definition
Section 4.25(e)(1)(i) of the TTB
regulations (27 CFR 4.25(e)(1)(i)) defines
a viticultural area for American wine as
a delimited grape-growing region
distinguishable by geographical
features, the boundaries of which have
been recognized and defined in part 9
of the regulations. These designations
allow vintners and consumers to
attribute a given quality, reputation, or
other characteristic of a wine made from
grapes grown in an area to its
geographic origin. The establishment of
viticultural areas allows vintners to
describe more accurately the origin of
their wines to consumers and helps
consumers to identify wines they may
PO 00000
Frm 00013
Fmt 4702
Sfmt 4702
purchase. Establishment of a viticultural
area is neither an approval nor an
endorsement by TTB of the wine
produced in that area.
Requirements
Section 4.25(e)(2) of the TTB
regulations outlines the procedure for
proposing an American viticultural area
and provides that any interested party
may petition TTB to establish a grapegrowing region as a viticultural area.
Section 9.3(b) of the TTB regulations
requires the petition to include—
• Evidence that the proposed
viticultural area is locally and/or
nationally known by the name specified
in the petition;
• Historical or current evidence that
supports setting the boundary of the
proposed viticultural area as the
petition specifies;
• Evidence relating to the
geographical features, such as climate,
soils, elevation, and physical features,
that distinguish the proposed
viticultural area from surrounding areas;
• A description of the specific
boundary of the proposed viticultural
area, based on features found on United
States Geological Survey (USGS) maps;
and
• A copy of the appropriate USGS
map(s) with the proposed viticultural
area’s boundary prominently marked.
Shawnee Hills Petition
TTB received a petition from Dr.
Theodore F. Wichmann, president of
Owl Creek Vineyard, Inc., and Dr. Imed
Dami, Illinois State Viticulturist,
proposing the establishment of a new
viticultural area in southern Illinois to
be called ‘‘Shawnee Hills.’’ The
proposed Shawnee Hills viticultural
area lies largely within the Shawnee
National Forest in Alexander, Gallatin,
Hardin, Jackson, Johnson, Pope, Pulaski,
Randolph, Saline, Union, and William
counties. Encompassing a region of
unglaciated hills between the Ohio and
Mississippi Rivers, the proposed
viticultural area is about 80 miles long
east to west and 20 miles wide north to
south, and it covers about 2,139 square
miles or 1,268,960 acres.
People have raised grapes, including
such important present-day wine
varieties as Norton, in the proposed
Shawnee Hills viticultural area since
1860, according to the petition, citing
‘‘Grape Culture’’ by W.E. Gould (1891).
The proposed area contained 1,250
acres of vineyards in 1890, and vintners
produced 19,750 gallons of wine in
1891, the petition adds, citing ‘‘Grape
and Wine Production in Illinois from
1983 to Present,’’ by R.M. Skirvin, et al.,
in ‘‘Illinois Grape Growers and Vintners
E:\FR\FM\08APP1.SGM
08APP1
Agencies
[Federal Register Volume 70, Number 67 (Friday, April 8, 2005)]
[Proposed Rules]
[Pages 17928-17940]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-7013]
========================================================================
Proposed Rules
Federal Register
________________________________________________________________________
This section of the FEDERAL REGISTER contains notices to the public of
the proposed issuance of rules and regulations. The purpose of these
notices is to give interested persons an opportunity to participate in
the rule making prior to the adoption of the final rules.
========================================================================
Federal Register / Vol. 70, No. 67 / Friday, April 8, 2005 / Proposed
Rules
[[Page 17928]]
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
9 CFR Parts 93, 94, and 98
[Docket No. 02-046-1]
RIN 0579-AB79
Importation of Swine and Swine Products From the European Union
AGENCY: Animal and Plant Health Inspection Service, USDA.
ACTION: Proposed rule.
-----------------------------------------------------------------------
SUMMARY: We are proposing to amend the regulations for importing
animals and animal products into the United States to apply a uniform
set of importation requirements related to classical swine fever (CSF)
to a region consisting of all of the 15 Member States of the European
Union (EU) that comprised the EU as of April 30, 2004 (the EU-15) and
prohibit for a specified period of time the importation of live swine
and swine products from any area in the EU-15 that is identified by the
veterinary authorities of the region as a restricted zone. We believe
these changes are necessary to help prevent the introduction of CSF
into the United States while increasing our responsiveness to changes
in the CSF situation in the EU.
DATES: We will consider all comments that we receive on or before June
7, 2005.
ADDRESSES: You may submit comments by any of the following methods:
EDOCKET: Go to https://www.epa.gov/feddocket to submit or
view public comments, access the index listing of the contents of the
official public docket, and to access those documents in the public
docket that are available electronically. Once you have entered
EDOCKET, click on the ``View Open APHIS Dockets'' link to locate this
document.
Postal Mail/Commercial Delivery: Please send four copies
of your comment (an original and three copies) to Docket No. 02-046-1,
Regulatory Analysis and Development, PPD, APHIS, Station 3C71, 4700
River Road Unit 118, Riverdale, MD 20737-1238. Please state that your
comment refers to Docket No. 02-046-1.
Federal eRulemaking Portal: Go to https://
www.regulations.gov and follow the instructions for locating this
docket and submitting comments.
Reading Room: You may read any comments that we receive on this
docket in our reading room. The reading room is located in room 1141 of
the USDA South Building, 14th Street and Independence Avenue SW.,
Washington, DC. Normal reading room hours are 8 a.m. to 4:30 p.m.,
Monday through Friday, except holidays. To be sure someone is there to
help you, please call (202) 690-2817 before coming.
Other Information: You may view APHIS documents published in the
Federal Register and related information on the Internet at https://
www.aphis.usda.gov/ppd/rad/webrepor.html.
FOR FURTHER INFORMATION CONTACT: Dr. Chip Wells, Senior Staff
Veterinarian, Regionalization Evaluation Services Staff, National
Center for Import and Export, VS, APHIS, 4700 River Road Unit 38,
Riverdale, MD 20737-1231; (301) 734-4356.
SUPPLEMENTARY INFORMATION:
Background
The Animal and Plant Health Inspection Service (APHIS) of the
United States Department of Agriculture (USDA or the Department)
regulates the importation of animals and animal products into the
United States to guard against the introduction of animal diseases not
currently present or prevalent in this country. The regulations in 9
CFR part 94 (referred to below as the regulations) prohibit or restrict
the importation of specified animals and animal products to prevent the
introduction into the United States of various animal diseases,
including classical swine fever (CSF), rinderpest, foot-and-mouth
disease, bovine spongiform encephalopathy, swine vesicular disease, and
African swine fever.
Sections 94.9 and 94.10 of the regulations state that CSF is known
to exist in all regions of the world, except for those regions listed
in Sec. Sec. 94.9(a) and 94.10(a). The importation of live swine and
swine products from regions not recognized as free of CSF is restricted
or prohibited. In addition, the importation of live swine and swine
products from a region consisting of certain Member States and portions
of Member States of the European Union (EU) is restricted with regard
to CSF, even though that region is listed as free of the disease. The
restrictions on imports from that region were established in a final
rule published in the Federal Register on April 7, 2003 (68 FR 16922-
16941, Docket No. 98-090-5).
We based our final rule primarily on two risk analyses conducted by
APHIS.1 2 The risk analyses examined a region consisting of
EU countries (Member States) that the European Commission (EC) asked us
to recognize as free of CSF. (The EC is the EU institution responsible
for representing the EU as a whole. It proposes legislation, policies,
and programs of action and implements decisions of the EU Parliament
and Council.) The Member States identified were Austria, Belgium,
France, Germany, Greece, Italy, Luxembourg, the Netherlands, Portugal,
and Spain. Five other EU Member States--Denmark, Finland, the Republic
of Ireland, Sweden, and the United Kingdom--were already recognized by
APHIS as being free of CSF.
---------------------------------------------------------------------------
\1\ Biological Risk Analysis: Risk assessment and management
options for imports of swine and swine products from the European
Union--June 2, 1999.
\2\ Risk Analysis for Importation of Classical Swine Fever Virus
in Swine and Swine Products from the European Union--December 2000.
---------------------------------------------------------------------------
The first risk analysis was made available to the public in 1999 at
the time of publication in the Federal Register of the proposed rule
(64 FR 34155-34168, Docket No. 98-090-1) upon which we based our April
2003 final rule. The second risk analysis was released in 2002 for
public comment (67 FR 22388-22389, Docket No. 98-090-2) and represented
a revision and supplementation of the 1999 risk analysis. Data used in
both risk analyses represented events that occurred during a CSF
epidemic in Europe during 1997 and 1998. That outbreak is considered to
be the most severe CSF epidemic ever experienced in Europe. Both risk
analyses are available by calling or writing to the person listed in
this
[[Page 17929]]
document under FOR FURTHER INFORMATION CONTACT. The analyses are also
available on the Internet at https://www.aphis.usda.gov/vs/ncie/reg-
request.html. At the bottom of that Web site page, click on
``Information previously submitted by Regions requesting export
approval and supporting documentation.'' At the next screen, click on
the triangle beside ``European Union/Not Specified/Classical Swine
Fever,'' then click on the triangle beside ``Response by APHIS,'' which
will reveal links to the risk analyses.
The analyses took into account, among other things, the CSF history
of the EU region consisting of the 10 Member States in the EC's
request, the CSF history of countries adjacent to the region, the
veterinary infrastructure and policies of the region, and the
historical volumes of imports into the United States of breeding swine,
swine semen, and pork and pork products from the region.
Based on the analyses, we considered it necessary to establish
certain mitigation measures for the importation of live swine, pork and
pork products, and swine semen from the region. Although there were no
CSF outbreaks in EU domestic swine within the defined region at the
time, the risk analyses assumed that, because CSF was endemic in wild
boar in several parts of the EU, it was likely CSF would continue to
occur in domestic swine in the region. Further, the risk analyses
considered the open borders among EU Member States. To address these
situations, the final rule required that commodities from the region of
the EU that was considered to be unaffected with CSF be segregated from
those from CSF-affected regions of the EU and other CSF-affected
regions, and that measures be taken to ensure that donor boars
providing semen for export to the United States are truly free of CSF.
These requirements are described below under the heading ``Importation
Conditions Established in April 2003.''
Importation Conditions Established in April 2003
Specifically, our April 2003 final rule required that the following
conditions be met before the commodity in question could be imported
into the United States (in the absence of any other diseases of swine
that would otherwise prohibit importation):
For pork and pork products: (1) The articles have not been
commingled with pork or pork products derived from swine that have been
in a region listed at the time as one in which CSF is known to exist;
(2) the swine from which the pork or pork products were derived have
not lived in a region listed at the time as one in which CSF is known
to exist, and have not transited such a region unless moved directly
through the region in a sealed means of conveyance with the seal
determined to be intact upon arrival at the point of destination; and
(3) the articles are accompanied by a certificate, issued by an
official of the national government of the region of origin, stating
that the above provisions have been met.
For breeding swine: The swine (1) have never lived in a
region listed at the time as one in which CSF is known to exist; (2)
have never transited such a region unless moved directly through the
region in a sealed means of conveyance with the seal determined to be
intact upon arrival at the point of destination; and (3) have never
been commingled with swine that have been in a region listed at the
time as one in which CSF is known to exist. Additionally, no equipment
or materials used in transporting the swine may have previously been
used for transporting swine ineligible for export to the United States
unless the equipment or materials first were cleaned and disinfected.
Lastly, the swine have to be accompanied by a certificate, issued by a
salaried veterinary officer of the national government of the country
of origin, stating that the above provisions have been met.
For swine semen: The donor boar meets the same conditions
as those listed above for breeding swine. Additionally, the following
conditions must be met: (1) The semen comes from a semen collection
center approved for export by the veterinary services of the national
government of the country of origin; (2) the donor boar is held in
isolation for at least 30 days prior to entering the semen collection
center, and, no more than 30 days prior to being held in isolation, is
tested with negative results using a CSF test approved by the Office
International des Epizooties (OIE) [also referred to as the World
Organisation of Animal Health]; and (3) the donor boar is observed by
the semen collection center veterinarian while at the center (including
at least a 40-day holding period at the center following collection of
the semen) and, along with all other swine at the center, exhibits no
clinical signs of CSF.
Under these conditions, we estimated that the risk of introducing
CSF through imports from the defined region would be as follows:
By importing breeding swine, most likely one incursion in
an average of 33,670 years.
By importing fresh pork, most likely one incursion in an
average of 22,676 years.
By importing swine semen, most likely one incursion in an
average of 8,090 years.
APHIS considered each of these risks to be low.
We continue to consider the mitigation measures established in our
April 2003 final rule to be necessary for the importation of breeding
swine, pork and pork products, and swine semen from the EU region we
recognized in that final rule, and to France and Spain, which were
added to that region following publication of the April 2003 final rule
in a final rule published on April 20, 2004 (69 FR 21042-21047, Docket
No. 98-090-7). Under this proposed rule, those requirements would
continue to apply.
Additionally, we are proposing to apply the measures established in
our April 2003 final rule to importations from five additional EU
Member States whose exports to the United States are free of CSF-
related restrictions (Denmark, Finland, the Republic of Ireland,
Sweden, and the United Kingdom [consisting of England, Scotland, Wales,
the Isle of Man, and Northern Ireland]), as well as to Luxembourg
(which is currently listed as a region in which CSF exists, due to an
outbreak of the disease following our June 1999 proposal) and all of
Germany and Italy. Currently, only portions of Germany and Italy are
recognized as free of CSF in our regulations. We would apply the same
mitigation measures to each of the areas described above because we
would recognize the combination of all of those areas of the EU as a
single region of low-risk for CSF, discussed below. The region would be
comprised of the 15 Member States comprising the EU as of April 30,
2004, which we refer to as the European Union-15 (EU-15). We would add
a definition of European Union-15 (EU-15) to Sec. Sec. 93.500, 94.0,
and 98.30.
We discuss below, under the heading ``Uniform Conditions for
Imports from the EU-15,'' our proposed application of uniform import
conditions to the EU-15 with regard to CSF. We then discuss the reasons
we believe the EU-15 qualifies as a region of low-risk for CSF under
the heading ``Basis for Recognition of an EU Region.''
Uniform Conditions for Imports From the EU-15
As noted above, we are proposing to recognize a single region for
CSF (the EU-15) that would consist of the following areas: (1) That
region of the EU we now recognize as being free of
[[Page 17930]]
CSF but from which imports of swine and swine products are subject to
specified restrictions; (2) Denmark, Finland, the Republic of Ireland,
Sweden, and the United Kingdom (consisting of England, Scotland, Wales,
the Isle of Man, and Northern Ireland); and (3) Luxembourg and all of
Germany and Italy. Currently, only portions of Germany and Italy are
recognized as free of CSF in our regulations.
In our April 2003 final rule, we did not include Denmark, Finland,
the Republic of Ireland, Sweden, and the United Kingdom in the EU
region we defined as free of classical swine fever but from which the
importation of swine and swine products are subject to certain
restrictions. Those five Member States had already been recognized in
previous rulemakings as regions in which CSF is not known to exist and
from which swine and swine products may be imported into the United
States without restriction related to CSF. We continued to treat those
Member States in the same way we had been treating them since the time
we recognized them as free of CSF; that is, we did not apply to them
the additional mitigation measures we were applying to the EU region we
recognized in the April 2003 final rule.
However, because we had recognized those five Member States as free
of CSF before the EU was established, the evaluations we had conducted
that supported such a classification of freedom did not take into
account the opening of national borders within the EU and the
possibility that the five CSF-free Member States would trade freely
with EU Member States that we considered CSF-affected.
As part of the EU, those five Member States carry out trade with
the rest of the EU under what is essentially an open-border trading
policy. There is no substantive difference between the way trade is
carried out within the EU by those five Member States compared to the
way it is carried out by other Member States. Because of these open-
border policies, we believe the CSF risk from the five member States
must be considered the same as from the EU region we recognized as
subject to additional mitigation measures in our April 2003 final rule,
and the same importation conditions would be applied to both areas
under this proposed rule.
Additionally, we are proposing to apply those importation
conditions to parts of the EU that we have not yet recognized as CSF-
free. In our April 2003 final rule, we excluded certain parts of the
EU--in some cases entire Member States--from the region we recognized
as CSF-free, either because those areas were not eligible for
recognition as CSF-free at the time we published the proposal for our
April 2003 final rule, or because they experienced an outbreak of CSF
in domestic swine following publication of that proposed rule. Those
areas included all of France and Spain--which have since been added to
the region of the EU we consider free of CSF with restrictions--all of
Luxembourg, and parts of Germany and Italy. In Germany, we excluded the
following kreis: the Kreis Uckermark in the Land of Brandenburg; the
Kreis Oldenberg, the Kreis Soltau-Fallingbostel, and the Kreis Vechta
in the Land of Lower Saxony; the Kreis Heinsberg and the Kreis
Warendorf in the Land of Northrhine-Westphalia; the Kreis Bernkastel-
Wittlich, the Kreis Bitburg-Pr[uuml]m, the Kreis Donnersbergkreis, the
Kreis Rhein-Hunsr[uuml]che, the Kreis S[uuml]dliche Weinstrasse, and
the Kreis Trier-Saarburg in the Land of Rhineland Palatinate; and the
Kreis Altmarkkreis in the Land of Saxony-Anhalt. In Italy, we excluded
the Regions of Emilia-Romagna, Piemonte, and Sardegna.
Whether we excluded an entire Member State or a smaller
administrative unit depended on whether we had identified in the June
1999 proposed rule the administrative unit we would recognize as a
region within a particular Member State in the event of a CSF outbreak.
We had identified such administrative units for Germany and Italy (the
``kreis'' in Germany and the ``region'' in Italy), but not for the
other Member States of the EU.
We are now proposing to apply the certification requirements
established by our April 2003 final rule to all the areas in Italy and
Germany listed above and to Luxembourg. In addition, we would require
the EC to certify that commodities (breeding swine, swine semen, and
fresh pork and pork products) are not exported from--and have not been
commingled with swine from--restricted zones in the EU during the
following time periods: (1) A period of 6 months after the last case of
CSF in domestic swine in the restricted zone; or (2) until restrictions
put in place by the EU because of CSF in wild boar in the restricted
zone are released. We consider this action warranted because we
consider the EU to be an homogeneous region of low CSF risk (although
one in which CSF outbreaks may continue to occur) and because the EC
has appropriate control measures in place to mitigate the risk of
continuing outbreaks.
We consider the EU to be homogeneous with regard to CSF despite the
fact that we have treated certain kreis in Germany and Regions in Italy
slightly differently from the rest of those countries during our
rulemaking process. Our June 1999 proposed rule excluded three kreis in
Germany and three Regions in Italy from consideration as part of the
region recognized in our April 2003 final rule. Because these areas had
experienced outbreaks within 6 months before collection of data for the
1999 risk analysis, the model excluded consideration of exports from
those areas. Exclusion of those areas was a policy decision based on
the regionalization approach being used by APHIS at the time.
However, the model used for the risk analysis was based on the
assumption that outbreaks would continue to occur in the EU. Even with
this assumption, the risk analysis concluded that the risk of exporting
CSF from the EU in breeding swine, swine semen, and fresh pork was low.
Outbreaks did, in fact, occur in some German kreis other than the three
excluded from the June 1999 proposed rule--as well as in France, Spain,
and Luxembourg, which were subject to the June 1999 proposed rule--and
to provide the public an opportunity to comment upon the outbreaks, we
did not include those kreis and Member States in our April 2003 final
rule. However, we consider the CSF risk posed by commodities from the
German kreis and Italian Regions that were excluded from the proposed
rule, as well as from those areas and Member States that had outbreaks
subsequent to the proposed rule, to be equivalent to the CSF risk from
the other EU-15 Member States (as discussed above, in April 2004 we
added France and Spain to the EU region we recognized in April 2003).
We consider the risk from the EU-15 as a whole to be within the
parameters of the risk analysis, and believe the risk from continuing
CSF outbreaks in any part of the EU-15 would be adequately mitigated by
the control mechanisms implemented in the EU.
Thus, we are proposing to apply the same import conditions for
swine and swine products with regard to CSF to a region consisting of
all of Austria, Belgium, Denmark, Finland, France, Germany, Greece,
Italy, Luxembourg, the Netherlands, Portugal, the Republic of Ireland,
Spain, Sweden, and the United Kingdom. The conditions for pork, pork
products, and live swine would be set forth in Sec. 94.24. The
conditions for swine semen would be set forth in Sec. 98.38.
[[Page 17931]]
The EU-15 as a Region of Low Risk for CSF
In evaluating the CSF risk from imports of breeding swine, swine
semen, and swine products from the EU-15, we took into consideration
the following characteristics of that region:
The region contains a known source of CSF risk (e.g.,
infected wild boar) that may spread the disease virus to EU domestic
swine, resulting in continuing outbreaks of CSF in the region, but
veterinary officials in the region have established risk mitigation
measures adequate to prevent widespread exposure and establishment of
the disease;
Specific mitigation measures in place include
surveillance, epidemiological investigations, diagnostic capability,
and emergency response capacity that are sufficient to identify the
disease, establish appropriate control zones, and implement all
measures necessary to effectively limit the spread of CSF from the
region; and
Veterinary officials maintain contingency plans defining
proactive approaches to CSF control: The veterinary officials have
sufficient legal powers, a detailed chain-of-command, and appropriate
resources, including emergency funds, laboratory staff, equipment and
infrastructure, to carry out a rapid and effective eradication
campaign; there is an instruction manual detailing all procedures,
instructions, and measures, including emergency vaccination plans if
deemed necessary, to be implemented in the event of a CSF outbreak; and
appropriate staff regularly receive training and conduct drills in CSF
diagnosis, control measures, and communication techniques.
Included in the EC request to APHIS that resulted in our April 7,
2003, final rule was a request that was made in the context of the
Veterinary Equivalence Agreement (VEA) between the United States and
the EU, which was enacted in 1998. (The stated objective of the VEA is
to facilitate trade in live animals and animal products between the EU
and the United States by establishing a mechanism for the recognition
of equivalence of sanitary measures, consistent with the protection of
public and animal health, and improve communication and cooperation on
sanitary issues.) The EC requested that APHIS adopt the EC approach to
regionalization for CSF. This would require APHIS to establish a new
approach to dealing with outbreaks of CSF in the EU-15. As a result of
our review of the information provided, we are proposing to establish a
new approach that will adopt many elements of the EC approach to
dealing with outbreaks of CSF in the EU-15. Rather than responding to
outbreaks through rulemakings specific to each outbreak, we are
proposing in this document to establish actions that we would take in
the event of a CSF outbreak in the region. Our proposal and the way in
which it differs from current practice is explained below. While the
approach we are proposing would, in this case, apply specifically to
the EU-15, we would accept requests and supporting information from
other regions interested in being considered for a similar approach.
Currently, Sec. 92.3 of the regulations provides that whenever the
EC establishes a quarantine for a disease in the EU in a region APHIS
recognizes as one in which the disease is not known to exist and the EC
imposes prohibitions or other restrictions on the movement of animals
or animal products from the quarantined area in the EU, such animals
and animal products are prohibited importation into the United States.
Additionally, APHIS published a final rule on May 4, 2004 (69 FR 25817-
25820, Docket No. 02-001-2) that established procedures to follow when
a region that we recognize as free of an animal disease experiences an
outbreak of that disease. If a region of the world that is considered
free of CSF experiences an outbreak of CSF, APHIS will prohibit or
restrict immediately the importation of live swine, fresh pork and pork
products, and swine semen from that region into the United States. We
then may publish an interim rule in the Federal Register as soon as
possible that removes that region from the lists in Sec. Sec. 94.9 and
94.10 of the regulations of regions in which CSF does not exist and
that prohibits or restricts, by regulation, the importation of live
swine, fresh pork and pork products, and swine semen. We accept public
comment on the interim rule for a specified period of time. If the
outbreak is eliminated in the region in question and a sufficient
amount of time passes (generally defined as consistent with OIE
recommendations) to ensure that the disease has been eradicated, we
evaluate the risk of resuming imports from the region. If we believe
the results of the risk evaluation support reinstatement of the
region's previous CSF-free status and resumption of the importation of
the prohibited swine and swine products into the United States, we make
the evaluation available to the public and solicit public comment on
it. If, after considering the public comments, we still consider it
warranted to reinstate the region's CSF-free status, we publish a final
rule in the Federal Register listing the region as free of CSF, and we
allow importations of swine and swine products to resume.
We are proposing in this document that, whenever an outbreak of CSF
occurs in the EU-15 and the competent veterinary authority of the EU-15
Member State establishes a quarantined area for CSF (also referred to
in this document as a ``restricted zone''), swine and swine products
will be prohibited importation into the United States from that zone.
No action would be required by APHIS; the prohibition would take effect
immediately. Swine and swine products would not be allowed importation
from the region unless they are accompanied by certification by an
official of the competent veterinary authority of the EU-15 Member
State that the prohibitions set forth in this proposed rule regarding
restricted zones (discussed below) have been met.
In the case of an outbreak of CSF in EU domestic swine, the
importation prohibitions would remain in effect for 6 months following
the depopulation of swine and the cleaning and disinfection of the last
infected premises in the restricted zone, even if the competent
veterinary authority of the EU-15 Member State removes its designation
of the area as a restricted zone before 6 months have elapsed. In the
case of a restricted zone established because of the detection of CSF
in wild boar, the importation prohibitions would remain in place until
the competent veterinary authority of the EU-15 Member State removes
its designation of the area as a restricted zone. (The issue of wild
boar is discussed further in this document under the heading ``Wild
Boar.'') The lifting of the prohibitions on imports into the United
States from a restricted zone would take effect at the times described
above. No action by APHIS would be required. However, APHIS would
reserve the right to make site visits and review documentation related
to the outbreak and eradication activities. In considering the CSF risk
in the EU-15, we evaluated both the ability of officials in that region
to ensure that such restricted zones would be effectively established
and maintained and the ability of the officials to ensure that
prohibitions on the importation into the United States of swine and
swine products from the restricted zones would be effectively enforced.
In Sec. Sec. 94.0 and 98.30, we would define restricted zone for
classical swine fever to mean an area, delineated by the relevant
competent veterinary authorities of the region in which the
[[Page 17932]]
area is located, that surrounds and includes the location of an
outbreak of CSF in domestic swine or detection of the disease in wild
boar, and from which the movement of domestic swine is prohibited. We
are not proposing to specify how far from an outbreak a restricted zone
must extend because factors such as geographic boundaries could
influence the necessary distance. However, we did evaluate the policies
of the EC for establishing restricted zones when considering whether to
consider the EU-15 as a region of low-risk for CSF. This is discussed
in more detail below under ``EU Animal Health Controls.''
We believe this new approach is warranted for the EU-15 because
that region has demonstrated the capability to effectively prevent the
spread of CSF from areas where outbreaks occur. Plus, as a
precautionary measure, imports of swine and swine products from the EU-
15 into the United States will be restricted to address the recognized
probability of these outbreaks occurring from time to time.
Because we are proposing to recognize the EU-15 as a single region
that poses a low risk for CSF, we would remove from Sec. Sec. 94.9(a)
and 94.10(a) of the regulations the EU-15 Member States currently
listed as regions in which CSF is not known to exist. The EU-15 would
be included in proposed Sec. Sec. 94.9(b) and 94.10(b) as a single
region of low-risk for CSF.
Basis for Consideration of the EU-15 as a Region of Low-Risk for CSF
We believe that consideration of the EU-15 as a single low-risk
region for CSF is warranted based on the risk analyses described above,
upon which we based on our April 2003 final rule, and on our knowledge
of the veterinary infrastructure and legislation in the EU. These
considerations are discussed in detail in an APHIS document titled
``APHIS Risk Considerations on Importation of Classical Swine Fever
(CSF) Virus in Breeding Swine, Swine Semen, and Fresh Pork from a
European Union Region of Fifteen Member States.'' The document can be
obtained by calling or writing to the person listed in this document
under FOR FURTHER INFORMATION CONTACT. It is also available on the
Internet at https://www.aphis.usda.gov/vs/ncie/reg-request.html. At the
bottom of that Web site page, click on ``Information previously
submitted by Regions requesting export approval and supporting
documentation.'' At the next screen, click on the triangle beside
``European Union/Not Specified/Classical Swine Fever,'' then click on
the triangle beside ``Response by APHIS,'' which will reveal a link to
the document.
The estimates of risk in the analyses we conducted regarding CSF in
the EU-15 suggest that the EU's control mechanisms, combined with the
risk mitigation measures we established in the April 2003 final rule,
are sufficiently effective to mitigate the risk of introducing the CSF
virus to the United States via exports of the swine and swine products
that would be eligible for importation into the United States under
this rule.
The risk estimated in the risk analyses regarding the EU that we
conducted in 1999 and 2000 was based on quantitative data reflecting
the effects of EU regulations that were in place during a severe CSF
outbreak in 1997 and 1998 that occurred extensively in the Netherlands
and that spread to other EU Member States. Although the outbreak was
considered the most severe the EU ever experienced and CSF did spread
during that outbreak, our quantitative estimates of risk showed that
the risk to the United States of CSF introduction due to that most
severe outbreak was low. Since that outbreak, the EU has implemented
measures to strengthen its response to a CSF outbreak. Therefore, with
the continued application of EU regulations, any risk from future CSF
outbreaks in the EU-15 is expected to also be low, unless an outbreak
occurs that is more severe than the one in 1997-1998--i.e., that poses
a risk greater than that evaluated in the analysis. In the event of a
more severe outbreak or any other circumstance the Administrator
considers to pose a risk (such as evidence of unreported CSF outbreaks
or significant deterioration of veterinary infrastructure or control in
the region), the APHIS Administrator would reserve the right to take
whatever action is necessary to ensure that CSF is not introduced into
the United States.
EU Animal Health Controls
In general, our proposed classification of the EU-15 as a region of
low risk for CSF is based on continued adherence in the Member States
to EU animal health controls, some of which are described below, as
well as on the measures we established in our April 2003 final rule.
However, in one way, we believe it is necessary to require a measure
that exceeds the EU controls. This measure has to do with the length of
time the prohibition on the importation into the United States of swine
and swine products from a restricted zone is maintained. We discuss
this measure at greater length below, under the heading ``Prohibition
of Importations from a Restricted Zone.''
Animal health regulations imposed in the EU are harmonized and
binding upon all Member States. Requirements include compulsory
notification of OIE List A diseases, including CSF, and laboratory
testing for CSF on all sick swine if CSF is suspected. Member States
are required to have CSF contingency plans and, if applicable,
eradication plans for CSF in wild boar populations.
Swine are moved freely among EU Member States and within Member
States. Swine born in one Member State are routinely fattened or
slaughtered in another. Animals moving between Member States are
required to be accompanied by an official health certificate issued by
an official veterinarian appointed by the competent veterinary
authority of the Member State. Prior notification of the movement is
reported electronically through an electronic network linking
authorities of the EC and Member States.\3\
---------------------------------------------------------------------------
\3\ TRACES (Trade Control and Export System) is replacing ANIMO
by the end of 2004 as the computerized system mandated by EU law to
track animal and animal product movement between Member States, as
well as to track imports from non-EU countries into the EU. Data are
entered by local veterinary authorities in each Member State and are
shared over a network with the rest of the EU. The system is
administered by a private contractor under the oversight of the EC
and the EU Court of Auditors.
---------------------------------------------------------------------------
Farm registration is mandatory, and each holding is assigned a
unique identification number by the competent veterinary authority of
the Member State. Animal identification is compulsory. Breeding swine
must be identified with a unique identification number (either by ear
tag or tattoo), and fattening swine must be identified by the holding
registration number. This information is maintained by each Member
State.
If CSF is detected anywhere in the EU, control mechanisms are
activated in accordance with EU legislation. When CSF is suspected on a
swine holding, a clinical investigation is conducted by the competent
veterinary authority of the Member State to confirm or rule out the
disease, and an epidemiological investigation is carried out. Movement
of swine from the holding under suspicion is prohibited, and
biosecurity measures are implemented to prevent spread of the disease.
If CSF is confirmed, all swine on the holding containing infected
swine must be depopulated, and the carcasses must be disposed of after
being treated to inactivate the CSF virus under official supervision.
Two types of zones are
[[Page 17933]]
established around an outbreak of CSF in EU domestic swine--
``protection zones'' and ``surveillance zones.'' The protection zone
extends at least 3 kilometers from the outbreak. The surveillance zone
extends at least 10 kilometers from the outbreak. For the purpose of
our regulations, we would consider the combination of an EU protection
zone and surveillance zone to constitute a restricted zone. When
establishing zones, the competent veterinary authority of the Member
State is required by EU legislation to take into account the following:
The results of the epidemiological investigation;
The geographical situation, particularly natural or
artificial boundaries;
The location and proximity of holdings;
Patterns of movements and trade in swine and the
availability of slaughterhouses;
The facilities and personnel available to control any
movement of swine within the zones, in particular if the swine to be
killed need to be moved away from their holding of origin.
Veterinary authorities are required to take all necessary measures,
including posting signs and alerting the media, to inform the public of
the imposed restrictions and must use appropriate measures to enforce
the restrictions. Veterinary authorities of Member States collaborate
in establishing zones that overlap their borders.
In accordance with EU regulations, premises located within the
protection zone are prohibited by the Member State from moving swine
out of that zone for at least 30 days following the depopulation of
swine and the cleaning and disinfection of the last premises in the
zone infected with CSF. Premises within the surveillance zone are
prohibited by the Member State from moving swine out of that zone for
at least 20 days following the depopulation of swine and the cleaning
and disinfection of the last premises in the protected zone infected
with CSF. A census is conducted of all swine in both the protection and
surveillance zones. Clinical examinations are conducted of all swine
within the protection zone.
An epidemiological inquiry is made into the origin of the virus in
the infected swine, and contacts are identified for traceback and
traceforward investigations. Isolates of the virus are genetically
typed by the EU Reference Laboratory in Hanover, Germany.
Under official supervision of the competent veterinary authority of
the Member State, meat of swine slaughtered during the period between
the probable introduction of disease and the implementation of control
measures is traced and processed in such a way as to destroy or
inactivate the CSF virus. Likewise, swine genetic products collected
during this time are traced and destroyed under official supervision in
such a way as to avoid the risk of spread of the CSF virus.
After the depopulation of swine, the buildings, equipment,
vehicles, and other articles that may have been contaminated with the
CSF virus must be cleaned and disinfected under official supervision
using approved disinfectants.
Swine may not be reintroduced onto a holding that contained
infected swine until at least 30 days after the required cleaning and
disinfection. Any swine reintroduced onto the holding must be monitored
to make sure that none develop antibodies to CSF.
The EU does not vaccinate domestic swine for CSF. However, with EC
approval, emergency vaccination may be used in cases where CSF has been
confirmed and epidemiological data suggest that the disease threatens
to spread.
Whenever CSF is detected in a wild boar, the competent veterinary
authority of the Member State, in consultation with an expert panel of
veterinarians, hunters, wildlife biologists, and epidemiologists,
defines the infected area, implements appropriate measures to reduce
the spread of the disease, develops and submits for EC approval an
eradication plan, and audit the effectiveness of measures adopted to
eradicate CSF from the infected area. These measures require that all
holdings of domestic swine in the infected area be placed under
official surveillance, an official census of swine be conducted, swine
movement be restricted, biosecurity measures be implemented, and
testing for CSF be conducted on all sick or dead swine. Further, all
wild boar shot or found dead must be examined and tested for CSF by an
official veterinarian designated by the competent veterinary authority
of the Member State. In addition, the measures taken may include
suspension of hunting and a ban on feeding wild boar. The veterinary
authority must also ensure that the CSF isolate is genetically typed.
Adjacent Member States collaborate in establishing control measures in
cases where the infected wild boar are found close to common borders.
As part of an approved eradication plan, emergency vaccination of
wild boar may be conducted in situations where CSF has been confirmed
and epidemiological data suggest that the disease threatens to spread.
The vaccination area must be part of the defined infected area, and
appropriate measures must be taken to prevent spread of the vaccine
virus to domestic swine. Currently, there is an ongoing emergency
vaccination program for wild boar in infected areas within Germany and
Luxembourg.
Requirement in Addition to EU Controls
As we stated above, we believe it is necessary to require a CSF
control measure in the EU-15 that exceeds EU controls and the
conditions imposed by our April 2003 final rule. This measure is the
length of time the prohibitions on the exportation of swine and swine
products to the United States are maintained. We discuss this measure
below.
Prohibition of Importations From a Restricted Zone
Current EU regulations allow CSF restrictions in a protection zone
(that area extending at least 3 kilometers from an infected holding of
domestic swine) to be removed 30 days after completion of preliminary
cleaning and disinfection measures on the infected holding.
Restrictions in a surveillance zone must stay in place at least 20 days
after such cleaning and disinfection. Restrictions are removed only
after clinical examinations and serology indicate that any swine
remaining in the area are free of CSF. Presumably, after restrictions
are released, swine from the area could be moved throughout the EU.
We are concerned by observations of recurrence of CSF in certain
areas shortly after such restrictions have been removed by the EU and
swine movement from the areas has commenced. For example, in December
2001, an outbreak was confirmed in Osoma, Spain, 22 days after release
of movement restrictions by the EU. In another case, an outbreak in
Luxembourg in August 2002 was epidemiologically linked to an outbreak
that occurred in June 2002, and occurred 27 days after release of
movement restrictions by the EU. During the 1997-1998 epidemic,
veterinary authorities in the EU usually found it necessary to maintain
movement restrictions for more than 30 days following an outbreak.
These observations suggest that restricting movement for only 30 days
may be insufficient to ensure that the region remains unaffected.
Further, as discussed below, we believe that OIE standards support
restriction of movement for more than 30 days. As discussed above, we
are
[[Page 17934]]
proposing to consider the EU-15 as a region of low risk for CSF, rather
than as a region in which CSF is not known to exist. The OIE standard
that would be relevant to such a region is the standard for a country
or zone free of CSF in domestic swine but with infection in the wild
swine population.\4\ In such situations, OIE recommends that, where a
stamping out policy without vaccination has been implemented for CSF
control, recognition of the region as CSF-free may be acquired 6 months
after the last outbreak in domestic swine.
---------------------------------------------------------------------------
\4\ OIE, Terrestrial Animal Health Code-2003, Part 2, Chapter
2.1.13.
---------------------------------------------------------------------------
We are in agreement with the OIE recommendation that restrictions
on the movement of swine and swine products from a CSF quarantined area
be maintained for 6 months, and consider it consistent with our
proposed consideration of the EU-15 as a region that poses a low risk
of CSF. Further, maintenance of such restrictions for 6 months is
consistent with our stated intent in our December 2000 risk analysis to
accept exports only from regions that have not experienced a CSF
outbreak within the previous 6 months.\5\ This is why we are proposing
to provide that our prohibition on the importation of swine and swine
products from a restricted zone established because of an outbreak of
CSF in domestic swine remain in place for at least 6 months following
the depopulation of swine and the cleaning and disinfection of the last
infected premises in the zone. As noted above, the prohibition of the
importation of swine and swine products from a restricted zone
established because of the detection of CSF in wild boar would remain
in place until the restricted zone status of the area is removed by the
competent veterinary authority of the EU-15 Member State.
---------------------------------------------------------------------------
\5\ Risk Analysis for Importation of Classical Swine Fever Virus
in Swine and Swine Products from the European Union--December 2000.
---------------------------------------------------------------------------
Wild Boar
Under our current regulations, we do not remove a region from the
lists in Sec. Sec. 94.9(a) and 94.10(a) of regions considered free of
CSF if the disease is detected in wild boar in the region but not in
domestic swine. This approach is consistent with APHIS domestic
regulations, which do not regulate wild boar in the United States for
swine diseases. However, under this proposed rule, we would prohibit
importations of swine and swine products from areas in the EU-15 placed
under quarantine by the competent veterinary authority of an EU-15
Member State because of the detection of CSF in wild boar, even if CSF
has not been detected in domestic swine in the area. Although the
estimates of CSF risk from the region identified in our 1999 and 2000
risk analyses were based on data related only to outbreaks and control
measures in EU domestic swine (i.e., data from wild boar outbreaks were
not included), we recognize that EU control measures implemented in
response to outbreaks in wild boar had a mitigating effect on the
spread of CSF in domestic swine. Therefore, we believe that EU control
measures for CSF in wild boar are a critical component of the overall
EU controls for CSF. Data indicate that wild boar continue to be a
potential source of infection in domestic swine. For example, infected
wild boar are the suspected source of virus linked to an August 2003
outbreak in Luxembourg, an April 2002 outbreak in France, and multiple
outbreaks in Germany. The EU recognizes the risk to its domestic swine
population because of the endemic CSF infection in wild boar and has
implemented eradication plans and contingency measures to deal with
this problem. To protect domestic swine herds throughout the region,
the EC has placed restrictions on movement of domestic swine from
infected wild boar areas. It is likely that the EU restrictions on
regions containing infected wild boar contribute significantly to the
effectiveness of EU control measures.
Certificate for Swine
Section 93.505 of the regulations requires that, except for swine
from Canada, all swine intended for importation into the United States
be accompanied by official certification regarding the health status of
the swine and the disease status of the region of origin. Paragraph (a)
of Sec. 93.505 requires that the certificate accompanying the swine
show that the entire region of origin of the swine is free of CSF. In
accordance with our proposed action to allow the importation of
breeding swine from the EU-15, we are proposing to change the language
in Sec. 93.505 accordingly, to allow for the importation of live swine
from the EU-15.
Application of this Approach to Other Regions
Section 92.2 of the regulations defines the type of information
that must be included with the request of a country or countries to
APHIS for recognition of the animal health status of a region.
Evaluation of this information would constitute the first step in
consideration of a new regulatory approach for the region. As part of
its consideration, APHIS would determine whether it might be
appropriate to revise its approach dealing with outbreaks in the region
that made the request. The results of these considerations will be
reflected in regulatory changes made through rulemaking. Aspects of the
rulemaking process are discussed in Sec. 92.2.
Authorized Inspectors
Currently, there is a requirement in Sec. 94.24(c) that
certificates required under Sec. 94.24 be presented by the importer of
swine and swine products to the appropriate Customs and Border
Protection officer at the port of arrival. We are proposing to require
instead that the certificates be presented to an authorized inspector,
which is defined in Sec. 94.0 as any individual authorized by the
Administrator of APHIS or the Commissioner of Customs and Border
Protection, Department of Homeland Security, to enforce the
regulations. This change would reflect the fact that, for some imports,
it is an APHIS employee who accepts the certificate at the port of
arrival.
Executive Order 12866 and Regulatory Flexibility Act
This proposed rule has been reviewed under Executive Order 12866.
The rule has been determined to be significant for the purposes of
Executive Order 12866 and, therefore, has been reviewed by the Office
of Management and Budget.
Under the Animal Health Protection Act (7 U.S.C. 8301 et seq.) the
Secretary of Agriculture is authorized to promulgate regulations to
prevent the introduction into the United States or dissemination of any
pest or disease of livestock. Under this authority, APHIS is proposing
to establish provisions for imports of swine and swine products from
the EU-15 under conditions we believe will guard against the
introduction of CSF into the United States from that region.
Below is the economic analysis for the changes proposed in this
document. The economic analysis provides a cost-benefit analysis as
required by Executive Order 12866 and an analysis of the potential
economic effects on small entities as required by the Regulatory
Flexibility Act.
We do not have enough data for a comprehensive analysis of the
economic effects of this proposed rule on small entities. Therefore, in
accordance with 5 U.S.C. 603, we have performed an initial regulatory
flexibility analysis for this proposed rule. We are inviting comments
about this proposed rule as it relates to small entities. In
particular, we are interested in determining the number and kind of
small entities who
[[Page 17935]]
may incur benefits or costs from implementation of this proposed rule
and the economic impact of those benefits or costs.
CSF is a highly contagious and fatal disease of swine. It was
eradicated from the United States in 1976 after a 16-year effort, at a
cost to USDA and individual States of about $140 million ($455 million
in 2003 dollars). The potential for reintroduction of CSF into the
United States remains a major concern, not only because of production
losses and eradication costs, but also because of the adverse effects
reintroduction would have on U.S. swine and pork exports.
APHIS determines, based on disease risk evaluations, whether
animals and animal products may be exported from foreign regions to the
United States. If a region recognized by APHIS as free of a specific
animal disease experiences an outbreak, generally an interim rule is
issued prohibiting or restricting potentially infected imports. Once
the outbreak has been eliminated, and a period of time has elapsed
sufficient to allow the animal disease situation in the region to
stabilize, the region's previous disease-free status may be restored.
APHIS personnel conduct a site visit and reevaluate the risk by
conducting a risk analysis. If, based on the analysis, APHIS believes
it is appropriate to once again consider the region free of the
disease, APHIS publishes a notice in the Federal Register soliciting
public comments on the analysis. Any comments received are reviewed and
each issue raised by commenters is considered. If, after review of the
comments, APHIS continues to consider it appropriate to once again
recognize the region free of the disease, a final rule is published in
the Federal Register giving notice of such recognition.
We believe this proposed rule would enable APHIS to respond more
quickly to changes in CSF conditions within the EU-15, while
maintaining the Agency's sanitary standards. The proposed rule would
change the procedure by which imports of swine, pork and pork products,
and swine semen would be allowed to resume following the elimination of
a CSF outbreak in the EU-15. Separate rulemaking would no longer be
required each time an area within the region experiences a CSF outbreak
and the disease is subsequently eliminated. Rather, APHIS would
recognize quarantine decisions made by the competent veterinary
authority of an EU-15 Member State and prohibit the importation of
swine and swine products from restricted zones in the EU-15 established
by the competent veterinary authority of an EU-15 Member State. As an
additional safeguard, imports of swine, fresh pork and pork products,
and swine semen into the United States from the restricted zone would
be prohibited for a period of 6 months following the depopulation of
swine and the cleaning and disinfection of the last infected premises
in the zone. Restrictions and prohibitions we would establish because
of the detection of CSF in wild boar would remain in place until the
restricted zone status of the area is removed by a competent veterinary
authority of the EU-15 Member State.
An alternative to the proposed rule would be to not change the
regulations--i.e., to continue to initiate rulemaking whenever the CSF
situation within the EU-15 changes. Continuing with the current
procedures would not achieve the Agency objective of improving the
Agency's responsiveness to CSF situation changes while maintaining
adequate disease prevention measures. A second alternative would be to
consider the EU-15 as a single region of low risk for CSF, but not
require that at least 6 months elapse after eradication of a disease
outbreak in the region before the importation of swine and swine
products into the United States could resume. This alternative would
forfeit the additional sanitary assurance that the 6-month period is
intended to provide to the U.S. swine industry that the reestablished
imports would be CSF-free. We believe that this proposed rule would be
preferable in allowing resumption of imports in a timelier manner,
while ensuring that sanitary standards are maintained. As noted above,
we invite public comment on this proposed rule, including comment on
how the proposed rule could be modified to reduce expected costs or
burdens for small entities consistent with its objectives. Any comment
suggesting changes to the proposed criteria should be supported by an
explanation of why the changes should be made.
Expected Effects of the Proposed Rule
This proposed rule could affect U.S. imports of swine, pork and
pork products, and swine semen from the EU-15 in several ways. One of
the effects would be potential additional restrictions on the
importation of swine semen from certain EU-15 Member States.
Additionally, the regulatory process used to establish import
restrictions for areas affected by CSF, and to remove those
restrictions when the disease is eliminated, would be simplified and
made timelier. We believe the proposed rule would also result in more
efficient use of APHIS resources. These areas of potential effects are
discussed in turn.
Change in Swine Semen Requirements
The EU-15 consists of the following Member States: Austria,
Belgium, Denmark, Finland, France, Germany, Greece, Italy, Luxembourg,
the Netherlands, Portugal, the Republic of Ireland, Spain, Sweden, and
the United Kingdom. APHIS considered five of the Member States--
Denmark, Finland, the Republic of Ireland, Sweden, and the United
Kingdom--to be free of CSF even before publication of our April 2003
final rule. In that final rule, we recognized--with the exception of
specified regions in Germany and Italy--the countries of Austria,
Belgium, Germany, Greece, Italy, the Netherlands, and Portugal as a
single region in which CSF is not known to exist. That final rule also
set forth conditions under which breeding swine, pork and pork
products, and swine semen could be imported into the United States from
that region.
The remaining three Member States-France, Luxembourg, and Spain-as
well as specified regions in Germany and in Italy, were not included in
the region recognized by the final rule because of outbreaks of CSF
either before or after publication of the June 1999 proposed rule on
which the April 2003 final rule was based. However, as discussed above,
we published a final rule in the Federal Register in April 2004 that
recognized France and Spain as part of the CSF-free region we had
established in our April 2003 final rule.
This proposed rule would consider the EU-15 to be a single region
of low-risk for CSF. Therefore, that region would include the seven
Member States we recognized in whole or in part as CSF-free in the
April 2003 final rule (Austria, Belgium, Germany, Greece, Italy, the
Netherlands, and Portugal), the five Member States we already
considered CSF-free before the April 2003 final rule (Denmark, Finland,
the Republic of Ireland, Sweden, and the United Kingdom), the two
Member States we recognized as CSF-free in our April 2004 final rule
(France and Spain), and Luxembourg. Under the provisions of this
proposed rule, each of the 15 Member States would be subject to the
import conditions set forth in the April 2003 final rule and to the
restrictions added in this document concerning waiting periods before
release of restrictions on zones where outbreaks have occurred. In
considering the effects of these changes, the key questions are: (1) In
what ways do the current import requirements for
[[Page 17936]]
Denmark, Finland, the Republic of Ireland, Sweden, and the United
Kingdom differ from the import requirements set forth in this proposed
rule; and (2) what effects would result for those five Member States
due to the changes in requirements for export to the United States?
This proposed rule prescribes conditions for the importation of
breeding swine, swine semen, and pork and pork products from areas
classified as low risk for CSF. Movement restrictions require that
there be no commingling of commodities intended for export to the
United States (or of the donor boars of swine semen intended for export
to the United States) with like commodities from areas where CSF is
known to exist. Movement of commodities intended for export to the
United States through areas where CSF is known to exist is permitted
only by sealed means of conveyance. Sanitary certification that these
provisions have been met is required.
Denmark, Finland, the Republic of Ireland, Sweden, and the United
Kingdom are already complying with the proposed conditions for pork,
pork products, and breeding swine, and, in fact, were meeting these
conditions before our April 2003 final rule. However, with respect to
swine semen, the proposal would require that before the semen is
exported to the United States, the donor boar must be held at the semen
collection center for at least 40 days following semen collection, to
ensure that the boar does not exhibit any clinical signs of CSF. This
would be a new risk mitigation measure for swine semen exported to the
United States from these five Member States.
Three of the five Member States, Denmark, the Republic of Ireland,
and the United Kingdom, have histories of swine semen exports to the
United States. From 1994 through 2002, the United States imported an
average of 2,474 straws of swine semen annually. The average yearly
share of U.S. swine semen imports supplied by the three Member States
over the 9-year period was about 26 percent. The United Kingdom was the
major source among the three Member States, supplying all of the three
Member States' swine semen exports to the United States in 5 of the 9
years.
Reportedly, donor boars are largely resident at swine collection
centers, so costs associated with the animals' maintenance would be
affected little by the 40-day holding period. A potential issue is
whether storage for 40 days before exportation would affect the quality
of the collected semen and therefore affect import demand. APHIS
welcomes information on this issue that may help in evaluating the
effect on swine semen importers.
More Timely Reestablishment of CSF-Free Status
The proposed procedure for reestablishing CSF-free status for an
area that has been under quarantine is expected to require less time
than current procedures, notwithstanding the 6-month restriction
following the last case of CSF and completion of disinfection measures.
More timely recognition of an area's CSF-free status would allow
imports of swine and swine products from the area to resume sooner than
at present. The effect of this procedural change would depend on the
difference in time required by the two regulatory approaches, and the
additional swine, swine meat, and swine genetics that would be imported
because of more timely recognition of an area's reestablished CSF-free
status.
APHIS published a final rule on May 4, 2004 (69 FR 25817-25820,
Docket No. 02-001-2) that codifies the procedures APHIS follows when a
region free of a particular disease has an outbreak and APHIS responds
to that outbreak by publishing an interim rule prohibiting or
restricting imports from that region. APHIS will reassess the disease
situation in that region, and, before taking any action to relieve or
finalize prohibitions or restrictions imposed by the interim rule, will
make information regarding its reassessment of the region's disease
status available to the public for comment. Based on that reassessment,
including comments received regarding the reassessment information,
APHIS will either publish a final rule reinstating the disease-free
status of the area, or a portion of the area covered by the interim
rule; publish an affirmation of the interim rule that imposed
prohibitions or restrictions on imports of animals and animal products
from