Concurrence With World Organization for Animal Health's Risk Designation for Bovine Spongiform Encephalopathy for Ireland, 60641-60642 [2022-21729]
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60641
Notices
Federal Register
Vol. 87, No. 193
Thursday, October 6, 2022
This section of the FEDERAL REGISTER
contains documents other than rules or
proposed rules that are applicable to the
public. Notices of hearings and investigations,
committee meetings, agency decisions and
rulings, delegations of authority, filing of
petitions and applications and agency
statements of organization and functions are
examples of documents appearing in this
section.
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection
Service
[Docket No. APHIS–2022–0005]
Concurrence With World Organization
for Animal Health’s Risk Designation
for Bovine Spongiform
Encephalopathy for Ireland
Animal and Plant Health
Inspection Service, Department of
Agriculture (USDA).
ACTION: Notice.
AGENCY:
We are advising the public of
our decision to concur with the World
Organization for Animal Health’s
(WOAH’s) bovine spongiform
encephalopathy (BSE) risk designation
for Ireland. The WOAH recognizes
Ireland as being of negligible risk for
BSE. We are taking this action based on
our review of information supporting
the WOAH’s risk designation for
Ireland.
SUMMARY:
Dr.
Rebecca Gordon, Senior Staff Officer,
Regionalization Evaluation Services,
Veterinary Services, APHIS, 920 Main
Campus Drive, Raleigh, NC, 27606;
(919) 855–7741; email:
AskRegionalization@usda.gov.
SUPPLEMENTARY INFORMATION: The
regulations in 9 CFR part 92 subpart B,
‘‘Importation of Animals and Animal
Products; Procedures for Requesting
BSE Risk Status Classification With
Regard To Bovines’’ (referred to below
as the regulations), set forth the process
by which the Animal and Plant Health
Inspection Service (APHIS) classifies
regions for bovine spongiform
encephalopathy (BSE) risk. Section 92.5
of the regulations provides that all
countries of the world are considered by
APHIS to be in one of three BSE risk
categories: Negligible risk, controlled
risk, or undetermined risk. These risk
categories are defined in § 92.1. Any
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FOR FURTHER INFORMATION CONTACT:
VerDate Sep<11>2014
17:46 Oct 05, 2022
Jkt 259001
region that is not classified by APHIS as
presenting either negligible risk or
controlled risk for BSE is considered to
present an undetermined risk. The list
of those regions classified by APHIS as
having either negligible risk or
controlled risk can be accessed on the
APHIS website at https://
www.aphis.usda.gov/aphis/ourfocus/
animalhealth/animal-and-animalproduct-import-information/animalhealth-status-of-regions. The list can
also be obtained by writing to APHIS at
Regionalization Evaluation Services,
Veterinary Services, APHIS, 4700 River
Road Unit 38, Riverdale, MD 20737–
1238.
Under the regulations, APHIS may
classify a region for BSE in one of two
ways. One way is for regions that have
not received a risk classification from
the World Organization for Animal
Health (WOAH) 1 to request
classification by APHIS. The other way
is for APHIS to concur with the
classification given to a country or
region by the WOAH.
If the WOAH has classified a region
as either BSE negligible risk or BSE
controlled risk, APHIS will seek
information to support concurrence
with the WOAH classification. This
information may be publicly available
information, or APHIS may request that
regions supply the same information
given to the WOAH. APHIS will
announce in the Federal Register,
subject to public comment, its intent to
concur with a WOAH classification.
In accordance with this process, we
published a notice 2 in the Federal
Register on April 14, 2022 (87 FR
22168- 22169, Docket No. APHIS–2022–
0005), in which we announced our
intent to concur with the WOAH risk
classification of Ireland as being a
region of negligible risk for BSE. We
solicited comments on the notice for 60
days ending on June 13, 2022. We
received one comment by that date,
from a private citizen.
The commenter claimed that we
provided no evidence to support that
BSE levels in Ireland’s cattle population
approach zero.
1 On May 28, 2022, the World Organization for
Animal Health announced a change to its acronym
from OIE to WOAH to match its full name. See
https://www.woah.org/en/the-world-organisationfor-animal-health-launches-its-refreshed-brandidentity/.
2 To view the notice, go to www.regulations.gov
and enter APHIS–2022–0005 in the Search field.
PO 00000
Frm 00001
Fmt 4703
Sfmt 4703
Neither the notice nor the conclusions
of the WOAH referenced in the notice
claimed that BSE cases in Ireland
approach zero. Rather, the WOAH
classified Ireland as BSE negligible risk.
While negligible risk indicates that the
occurrence of BSE is very rare, it does
not translate to zero risk, nor does it
imply the expectation or assumption
that the risk will become zero in the
future. Atypical BSE may still be
detected in countries or regions with a
negligible risk status. The atypical BSE
forms, L-type and H-type, occur
spontaneously at very low levels in all
cattle populations.
The commenter also stated that
relying on slaughterhouses/abattoirs to
find cases of BSE is an unreliable
surveillance method.
Because there is currently no test to
detect BSE in a live animal, sampling
for BSE is often performed in the
slaughterhouse/abattoir environment. It
may also be performed at rendering or
salvage facilities, on-farm, at veterinary
clinics, or at veterinary diagnostic
laboratories. Ireland provided
documentation for the standard
operating procedures for active
surveillance for BSE in cattle and
documented that the samples collected
are representative of the cattle
population in the country. Furthermore,
Ireland provided documentation that
BSE surveillance exceeded Type B
surveillance minimum requirements in
Chapter 11.4 of the WOAH Terrestrial
Animal Health Code. As the commenter
provided no information to support the
claim that this surveillance is
unreliable, we continue to concur with
the WOAH risk classification of Ireland
as being a region of negligible risk for
BSE.
The commenter also claimed that
laboratories in general lack the skills
necessary to detect BSE.
All BSE confirmatory testing in
Ireland is carried out in the Central
Veterinary Research Laboratory in
Backweston, which is the National
Reference Laboratory (NRL) for
transmissible spongiform
encephalopathies in Ireland. The
confirmatory tests used are
histopathology, immunohistochemistry
using antibody F89, and immunoblot
(Biorad TeSeE). All confirmatory and
discriminatory tests used are accredited
to the international standard for
laboratories (IS0–17025). All rapid
E:\FR\FM\06OCN1.SGM
06OCN1
60642
Federal Register / Vol. 87, No. 193 / Thursday, October 6, 2022 / Notices
screening for BSE is conducted with
European Union-approved rapid tests at
Rapid Test Laboratories that are
approved and monitored by the NRL.
Ireland provided documentation that
BSE diagnostic procedures and the
reference laboratory facilities (NRL and
Rapid Test Laboratories) meet the
requirements in the WOAH Manual of
Diagnostic Tests and Vaccines for
Terrestrial Animals. As the commenter
provided no information to support the
claim that these laboratories or tests are
unable to accurately detect BSE, we
continue to concur with the WOAH risk
classification of Ireland as being a
region of negligible risk for BSE.
Therefore, in accordance with the
regulations in § 92.5, we are
announcing our decision to concur with
the WOAH risk classification for
Ireland.
Congressional Review Act
Pursuant to the Congressional Review
Act (5 U.S.C. 801 et seq.), the Office of
Information and Regulatory Affairs
designated this action as not a major
rule, as defined by 5 U.S.C. 804(2).
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.
Done in Washington, DC, this 30th day of
September 2022.
Anthony Shea,
Administrator, Animal and Plant Health
Inspection Service.
[FR Doc. 2022–21729 Filed 10–5–22; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF COMMERCE
Census Bureau
Agency Information Collection
Activities; Submission to the Office of
Management and Budget (OMB) for
Review and Approval; Comment
Request; Monthly Wholesale Trade
Survey
Census Bureau, Commerce.
Notice of information collection,
request for comment.
AGENCY:
ACTION:
The Department of
Commerce, in accordance with the
Paperwork Reduction Act (PRA) of
1995, invites the general public and
other Federal agencies to comment on
proposed, and continuing information
collections, which helps us assess the
impact of our information collection
requirements and minimize the public’s
reporting burden. The purpose of this
notice is to allow for 60 days of public
comment on the proposed extension of
the Monthly Wholesale Trade Survey,
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SUMMARY:
VerDate Sep<11>2014
17:46 Oct 05, 2022
Jkt 259001
prior to the submission of the
information collection request (ICR) to
OMB for approval.
DATES: To ensure consideration,
comments regarding this proposed
information collection must be received
on or before December 5, 2022.
ADDRESSES: Interested persons are
invited to submit written comments by
email to Thomas.J.Smith@census.gov.
Please reference Monthly Wholesale
Trade Survey in the subject line of your
comments. You may also submit
comments, identified by Docket Number
USBC–2022–0016, to the Federal eRulemaking Portal: https://
www.regulations.gov. All comments
received are part of the public record.
No comments will be posted to https://
www.regulations.gov for public viewing
until after the comment period has
closed. Comments will generally be
posted without change. All Personally
Identifiable Information (for example,
name and address) voluntarily
submitted by the commenter may be
publicly accessible. Do not submit
Confidential Business Information or
otherwise sensitive or protected
information. You may submit
attachments to electronic comments in
Microsoft Word, Excel, or Adobe PDF
file formats.
FOR FURTHER INFORMATION CONTACT:
Requests for additional information or
specific questions related to collection
activities should be directed to Rebecca
Weaver, Chief, Wholesale Indicator
Branch, Economic Indicators Division,
301–763–9538, rebecca.l.weaver@
census.gov.
SUPPLEMENTARY INFORMATION:
I. Abstract
The Monthly Wholesale Trade Survey
(MWTS) provides measures of monthly
sales, end-of-month inventories, and
inventories/sales ratios in the United
States by selected kinds of business for
merchant wholesalers, excluding
manufacturers’ sales branches and
offices. Estimates from the MWTS are
released in three different reports each
month. High level aggregate estimates
for end-of-month inventories are first
released as part of the Advance
Economic Indicators Report
approximately 27 days after the close of
the reference month. The full Monthly
Wholesale Trade Report containing both
sales and inventories estimates is
released approximately 39 days after the
close of the reference month. Sales and
inventories estimates from the MWTS
are also released as part of the
Manufacturing and Trade Inventories
and Sales (MTIS) report issued
approximately 45 days after the close of
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Frm 00002
Fmt 4703
Sfmt 4703
the reference month. The Bureau of
Economic Analysis uses this
information to improve the inventory
valuation adjustments applied to
estimates of the Gross Domestic
Product. The Bureau of Labor Statistics
(BLS) uses the data as input to develop
Producer Price Indexes and productivity
measurements.
The MWTS sales estimates are also
used as an input in the Monthly Real
Dollar Estimates of Wholesale Sales
experimental product, first published on
September 19, 2022, which is a
supplement to the MWTS report. The
estimates were created from the nominal
MWTS sales series using product
weights developed from existing Census
Bureau data releases and price indexes
from the BLS. Within the report, real
dollar sales estimates and corresponding
residuals are available for Total
Merchant Wholesalers, except
Manufacturers’ Sales Branches and
Offices, as well as the two 3-digit and
eighteen 4-digit North American
Industry Classification System (NAICS)
wholesale subsectors. Monthly
estimates are available from January
2012 forward.
Estimates produced from the MWTS
are based on a probability sample and
are published on the NAICS basis. The
sample design consists of small,
medium, and large cases requested to
report sales and inventories each month.
The sample, consisting of about 4,200
wholesale businesses, is drawn from the
Business Register, which contains all
Employer Identification Numbers (EINs)
and listed establishment locations. The
sample is updated quarterly to reflect
employer business ‘‘births’’ and
‘‘deaths’’. New employer businesses
identified in the Business and
Professional Classification Survey are
added and employer businesses
determined to be no longer active are
removed.
II. Method of Collection
Respondents are initially contacted
primarily by email, with a small subset
receiving a form by mail. After initial
contact, non-respondents are contacted
by email and/or telephone follow-up.
We collect the data primarily by
internet. We collect a small portion of
the data by mail, telephone follow-up,
and fax.
III. Data
OMB Control Number: 0607–0190.
Form Number(s): SM4217–A and
SM4217–E.
Type of Review: Regular submission.
Request for an Extension, without
Change, of a Currently Approved
Collection.
E:\FR\FM\06OCN1.SGM
06OCN1
Agencies
[Federal Register Volume 87, Number 193 (Thursday, October 6, 2022)]
[Notices]
[Pages 60641-60642]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-21729]
========================================================================
Notices
Federal Register
________________________________________________________________________
This section of the FEDERAL REGISTER contains documents other than rules
or proposed rules that are applicable to the public. Notices of hearings
and investigations, committee meetings, agency decisions and rulings,
delegations of authority, filing of petitions and applications and agency
statements of organization and functions are examples of documents
appearing in this section.
========================================================================
Federal Register / Vol. 87, No. 193 / Thursday, October 6, 2022 /
Notices
[[Page 60641]]
DEPARTMENT OF AGRICULTURE
Animal and Plant Health Inspection Service
[Docket No. APHIS-2022-0005]
Concurrence With World Organization for Animal Health's Risk
Designation for Bovine Spongiform Encephalopathy for Ireland
AGENCY: Animal and Plant Health Inspection Service, Department of
Agriculture (USDA).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: We are advising the public of our decision to concur with the
World Organization for Animal Health's (WOAH's) bovine spongiform
encephalopathy (BSE) risk designation for Ireland. The WOAH recognizes
Ireland as being of negligible risk for BSE. We are taking this action
based on our review of information supporting the WOAH's risk
designation for Ireland.
FOR FURTHER INFORMATION CONTACT: Dr. Rebecca Gordon, Senior Staff
Officer, Regionalization Evaluation Services, Veterinary Services,
APHIS, 920 Main Campus Drive, Raleigh, NC, 27606; (919) 855-7741;
email: [email protected].
SUPPLEMENTARY INFORMATION: The regulations in 9 CFR part 92 subpart B,
``Importation of Animals and Animal Products; Procedures for Requesting
BSE Risk Status Classification With Regard To Bovines'' (referred to
below as the regulations), set forth the process by which the Animal
and Plant Health Inspection Service (APHIS) classifies regions for
bovine spongiform encephalopathy (BSE) risk. Section 92.5 of the
regulations provides that all countries of the world are considered by
APHIS to be in one of three BSE risk categories: Negligible risk,
controlled risk, or undetermined risk. These risk categories are
defined in Sec. 92.1. Any region that is not classified by APHIS as
presenting either negligible risk or controlled risk for BSE is
considered to present an undetermined risk. The list of those regions
classified by APHIS as having either negligible risk or controlled risk
can be accessed on the APHIS website at https://www.aphis.usda.gov/aphis/ourfocus/animalhealth/animal-and-animal-product-import-information/animal-health-status-of-regions. The list can also be
obtained by writing to APHIS at Regionalization Evaluation Services,
Veterinary Services, APHIS, 4700 River Road Unit 38, Riverdale, MD
20737-1238.
Under the regulations, APHIS may classify a region for BSE in one
of two ways. One way is for regions that have not received a risk
classification from the World Organization for Animal Health (WOAH) \1\
to request classification by APHIS. The other way is for APHIS to
concur with the classification given to a country or region by the
WOAH.
---------------------------------------------------------------------------
\1\ On May 28, 2022, the World Organization for Animal Health
announced a change to its acronym from OIE to WOAH to match its full
name. See https://www.woah.org/en/the-world-organisation-for-animal-health-launches-its-refreshed-brand-identity/.
---------------------------------------------------------------------------
If the WOAH has classified a region as either BSE negligible risk
or BSE controlled risk, APHIS will seek information to support
concurrence with the WOAH classification. This information may be
publicly available information, or APHIS may request that regions
supply the same information given to the WOAH. APHIS will announce in
the Federal Register, subject to public comment, its intent to concur
with a WOAH classification.
In accordance with this process, we published a notice \2\ in the
Federal Register on April 14, 2022 (87 FR 22168- 22169, Docket No.
APHIS-2022-0005), in which we announced our intent to concur with the
WOAH risk classification of Ireland as being a region of negligible
risk for BSE. We solicited comments on the notice for 60 days ending on
June 13, 2022. We received one comment by that date, from a private
citizen.
---------------------------------------------------------------------------
\2\ To view the notice, go to www.regulations.gov and enter
APHIS-2022-0005 in the Search field.
---------------------------------------------------------------------------
The commenter claimed that we provided no evidence to support that
BSE levels in Ireland's cattle population approach zero.
Neither the notice nor the conclusions of the WOAH referenced in
the notice claimed that BSE cases in Ireland approach zero. Rather, the
WOAH classified Ireland as BSE negligible risk. While negligible risk
indicates that the occurrence of BSE is very rare, it does not
translate to zero risk, nor does it imply the expectation or assumption
that the risk will become zero in the future. Atypical BSE may still be
detected in countries or regions with a negligible risk status. The
atypical BSE forms, L-type and H-type, occur spontaneously at very low
levels in all cattle populations.
The commenter also stated that relying on slaughterhouses/abattoirs
to find cases of BSE is an unreliable surveillance method.
Because there is currently no test to detect BSE in a live animal,
sampling for BSE is often performed in the slaughterhouse/abattoir
environment. It may also be performed at rendering or salvage
facilities, on-farm, at veterinary clinics, or at veterinary diagnostic
laboratories. Ireland provided documentation for the standard operating
procedures for active surveillance for BSE in cattle and documented
that the samples collected are representative of the cattle population
in the country. Furthermore, Ireland provided documentation that BSE
surveillance exceeded Type B surveillance minimum requirements in
Chapter 11.4 of the WOAH Terrestrial Animal Health Code. As the
commenter provided no information to support the claim that this
surveillance is unreliable, we continue to concur with the WOAH risk
classification of Ireland as being a region of negligible risk for BSE.
The commenter also claimed that laboratories in general lack the
skills necessary to detect BSE.
All BSE confirmatory testing in Ireland is carried out in the
Central Veterinary Research Laboratory in Backweston, which is the
National Reference Laboratory (NRL) for transmissible spongiform
encephalopathies in Ireland. The confirmatory tests used are
histopathology, immunohistochemistry using antibody F89, and immunoblot
(Biorad TeSeE). All confirmatory and discriminatory tests used are
accredited to the international standard for laboratories (IS0-17025).
All rapid
[[Page 60642]]
screening for BSE is conducted with European Union-approved rapid tests
at Rapid Test Laboratories that are approved and monitored by the NRL.
Ireland provided documentation that BSE diagnostic procedures and the
reference laboratory facilities (NRL and Rapid Test Laboratories) meet
the requirements in the WOAH Manual of Diagnostic Tests and Vaccines
for Terrestrial Animals. As the commenter provided no information to
support the claim that these laboratories or tests are unable to
accurately detect BSE, we continue to concur with the WOAH risk
classification of Ireland as being a region of negligible risk for BSE.
Therefore, in accordance with the regulations in Sec. 92.5, we are
announcing our decision to concur with the WOAH risk classification for
Ireland.
Congressional Review Act
Pursuant to the Congressional Review Act (5 U.S.C. 801 et seq.),
the Office of Information and Regulatory Affairs designated this action
as not a major rule, as defined by 5 U.S.C. 804(2).
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.
Done in Washington, DC, this 30th day of September 2022.
Anthony Shea,
Administrator, Animal and Plant Health Inspection Service.
[FR Doc. 2022-21729 Filed 10-5-22; 8:45 am]
BILLING CODE 3410-34-P