Agency Information Collection Activities; Proposed Collection; Comment Request; Regulations Under the Federal Import Milk Act, 30951-30953 [05-10703]
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Federal Register / Vol. 70, No. 103 / Tuesday, May 31, 2005 / Notices
negotiation of fees. By orchestrating
agreements among its members to deal
only on collectively-determined terms,
and actual or threatened refusals to deal
with health plans that would not agree
to those terms, San Juan IPA violated
Section 5 of the FTC Act.
The Proposed Consent Order
The proposed order is designed to
remedy the illegal conduct charged in
the complaint and prevent its
recurrence. It is similar to recent
consent orders that the Commission has
issued to settle charges that physician
groups engaged in unlawful agreements
to raise fees they receive from health
plans.
The proposed order’s specific
provisions are as follows:
Paragraph II.A prohibits San Juan IPA
from entering into or facilitating any
agreement between or among any
physicians: (1) To negotiate with payors
on any physician’s behalf; (2) to deal,
not to deal, or threaten not to deal with
payors; (3) on what terms to deal with
any payor; or (4) not to deal
individually with any payor, or to deal
with any payor only through an
arrangement involving San Juan IPA.
Other parts of Paragraph II reinforce
these general prohibitions. Paragraph
II.B prohibits San Juan IPA from
facilitating exchanges of information
between physicians concerning
whether, or on what terms, to contract
with a payor. Paragraph II.C bars
attempts to engage in any action
prohibited by Paragraph II.A or II.B, and
Paragraph II.D proscribes inducing
anyone to engage in any action
prohibited by Paragraphs II.A through
II.C.
As in other Commission orders
addressing providers’ collective
bargaining with health care purchasers,
certain kinds of agreements are
excluded from the general bar on joint
negotiations. San Juan IPA would not be
precluded from engaging in conduct
that is reasonably necessary to form or
participate in legitimate joint
contracting arrangements among
competing physicians in a ‘‘qualified
risk-sharing joint arrangement’’ or a
‘‘qualified clinically-integrated joint
arrangement.’’ The arrangement,
however, must not facilitate the refusal
of, or restrict, physicians in contracting
with payors outside of the arrangement.
As defined in the proposed order, a
‘‘qualified risk-sharing joint
arrangement’’ possesses two key
characteristics. First, all physician
participants must share substantial
financial risk through the arrangement,
such that the arrangement creates
incentives for the physician participants
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Jkt 205001
jointly to control costs and improve
quality by managing the provision of
services. Second, any agreement
concerning reimbursement or other
terms or conditions of dealing must be
reasonably necessary to obtain
significant efficiencies through the joint
arrangement.
A ‘‘qualified clinically-integrated joint
arrangement,’’ on the other hand, need
not involve any sharing of financial risk.
Instead, as defined in the proposed
order, physician participants must
participate in active and ongoing
programs to evaluate and modify their
clinical practice patterns in order to
control costs and ensure the quality of
services provided, and the arrangement
must create a high degree of
interdependence and cooperation
among physicians. As with qualified
risk-sharing arrangements, any
agreement concerning price or other
terms of dealing must be reasonably
necessary to achieve the efficiency goals
of the joint arrangement.
Paragraph III, for three years, requires
San Juan IPA to notify the Commission
before participating in contracting with
health plans on behalf of a qualified
risk-sharing joint arrangement or a
qualified clinically-integrated joint
arrangement. Paragraph III also sets out
the information necessary to make the
notification complete.
Paragraph IV, for three years, requires
San Juan IPA to notify the Commission
before entering into any arrangement to
act as a messenger, or as an agent on
behalf of any physicians, with payors
regarding contracts. Paragraph IV also
sets out the information necessary to
make the notification complete.
Paragraph V.A requires San Juan IPA
to distribute the complaint and order to
all physicians who have participated in
San Juan IPA, and to payors that
negotiated contracts with San Juan IPA
or indicated an interest in contracting
with San Juan IPA. Paragraph V.B
requires San Juan IPA, at any payor’s
request and without penalty, or, at the
latest, within one year after the order is
made final, to terminate its current
contracts. Paragraph V.C requires San
Juan IPA to distribute payor requests for
contract termination to all physicians
who participate in San Juan IPA.
Paragraph V.D.1.b requires San Juan IPA
to distribute the complaint and order to
any payors that negotiate contracts with
San Juan IPA in the next three years.
Paragraphs VI and VII of the proposed
order impose various obligations on San
Juan IPA to report or provide access to
information to the Commission to
facilitate monitoring San Juan IPA’s
compliance with the order.
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30951
The proposed order will expire in 20
years.
By direction of the Commission, Chairman
Majoras not participating.
Donald S. Clark,
Secretary.
[FR Doc. 05–10682 Filed 5–27–05; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2005N–0178]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Regulations Under
the Federal Import Milk Act
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
reporting and recordkeeping
requirements in implementing the
Federal Import Milk Act (FIMA).
DATES: Submit written or electronic
comments on the collection of
information by August 1, 2005.
ADDRESSES: Submit electronic
comments on the collection of
information to: https://www.fda.gov/
dockets/ecomments. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Peggy Robbins, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–1223.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
E:\FR\FM\31MYN1.SGM
31MYN1
30952
Federal Register / Vol. 70, No. 103 / Tuesday, May 31, 2005 / Notices
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Regulations Under the Federal Import
Milk Act—21 CFR Part 1210 (OMB
Control Number 0910–0212)—Extension
Under the regulations implementing
FIMA (21 U.S.C. 141–149), milk or
cream may be imported into the United
States only by the holder of a valid
import milk permit. Before such permit
is issued: (1) All cows from which
import milk or cream is produced must
be physically examined and found
healthy; (2) if the milk or cream is
imported raw, all such cows must pass
a tuberculin test; (3) the dairy farm and
each plant in which the milk or cream
is processed or handled must be
inspected and found to meet certain
sanitary requirements; (4) bacterial
counts of the milk at the time of
importation must not exceed specified
limits; and (5) the temperature of the
milk or cream at time of importation
must not exceed 50° F. In addition, the
regulations in part 1210 (21 CFR part
1210) require that dairy farmers and
plants maintain pasteurization records
(§ 1210.15) and that each container of
milk or cream imported into the United
States bear a tag with the product type,
permit number, and shipper’s name and
address (§ 1210.22).
FDA estimates the burden of this
collection of information as follows:
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
21 CFR
Section
Form No.
No. of
Respondents
Annual
Frequency
per Response
Total Annual
Responses
Hours per
Response
Total Hours
FDA 1815/Permits granted on certificates
1210.23
8
1
8
0.5
4.0
FDA 1993/Application of permit
1210.20
8
1
8
0.5
4.0
FDA 1994/Tuberculin test
1210.13
1
1
1
0.5
0.5
FDA 1995/Physical examination of
cows
1210.12
1
1
1
0.5
0.5
FDA 1996/Sanitary inspection of dairy
farms
1210.11
8
200
1,600
1.5
2,400
FDA 1997/Sanitary inspections of
plants
1210.14
8
1
8
2.0
16.0
Total
1There
2,425.0
are no capital costs or operating and maintenance costs associated with this collection of information.
TABLE 2.—ESTIMATED ANNUAL RECORDKEEPING BURDEN1
21 CFR Section
No. of
Recordkeepers
1210.15
1There
Annual Frequency per
Recordkeeping
Total Annual Records
1
Hours per
Record
8
8
Total Hours
0.05
0.40
are no capital costs or operating and maintenance costs associated with this collection of information.
These estimates are based on the
number of current permit holders and
the number of inquiries that FDA has
received regarding requests for
applications in the past 3 years. No
burden has been estimated for the
tagging requirement in § 1210.22
because the information on the tag is
either supplied by FDA (permit number)
or is disclosed to third parties as a usual
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16:14 May 27, 2005
Jkt 205001
and customary part of the shipper’s
normal business activities (type of
product, shipper’s name and address).
Under 5 CFR 1320.3(c)(2), the public
disclosure of information originally
supplied by the Federal Government to
the recipient for the purpose of
disclosure to the public is not a
collection of information. Under 5 CFR
1320.3(b)(2)), the time, effort, and
PO 00000
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Fmt 4703
Sfmt 4703
financial resources necessary to comply
with a collection of information are
excluded from the burden estimate if
the reporting, recordkeeping, or
disclosure activities needed to comply
are usual and customary because they
would occur in the normal course of
activities. Low burden has been
estimated for Forms FDA 1994 and 1995
because they are not are not used often.
E:\FR\FM\31MYN1.SGM
31MYN1
Federal Register / Vol. 70, No. 103 / Tuesday, May 31, 2005 / Notices
The Secretary of Health and Human
Services has the discretion to allow
Form FDA 1815, a duly certified
statement signed by an accredited
official of a foreign government, to be
submitted in lieu of Forms FDA 1994
and 1995. To date, Form FDA 1815 has
been submitted in lieu of these forms.
Dated: May 17, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05–10703 Filed 5–27–05; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2005D–0174]
Draft Guidance on Expiration Dating of
Unit-Dose Repackaged Drugs;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of a draft guidance entitled
‘‘Expiration Dating of Unit-Dose
Repackaged Drugs.’’ The draft guidance
is a proposed revision of section
480.200 of FDA’s Compliance Policy
Guide (CPG) (CPG 7132b.11). We are
proposing to revise CPG 7132b.11 so
that FDA enforcement policy regarding
expiration dating of nonsterile unit-dose
repackaged drugs under the agency’s
current good manufacturing practice
(CGMP) regulations is substantially
comparable to the expiration dating
standards for such drugs set forth in the
U.S. Pharmacopeia (USP).
DATES: Submit written or electronic
comments on the draft guidance by
August 29, 2005. General comments on
agency guidance documents are
welcome at any time.
ADDRESSES: Submit written requests for
single copies of the draft guidance to the
Division of Drug Information (HFD–
240), Center for Drug Evaluation and
Research, Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857. Send one selfaddressed adhesive label to assist that
office in processing your requests.
Submit written comments on the draft
guidance to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Submit
electronic comments to https://
www.fda.gov/dockets/ecomments. See
the SUPPLEMENTARY INFORMATION section
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16:14 May 27, 2005
Jkt 205001
for electronic access to the draft
guidance document.
FOR FURTHER INFORMATION CONTACT:
Barry Rothman, Center for Drug
Evaluation and Research (HFD–320),
Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857,
301–827–9026.
SUPPLEMENTARY INFORMATION:
I. Background
We are announcing the availability of
a draft guidance on ‘‘Expiration Dating
of Unit-Dose Repackaged Drugs.’’ The
document provides guidance on FDA’s
enforcement policy regarding expiration
dating of repackaged nonsterile solid
and liquid unit-dose drugs under
§ 211.137 (21 CFR 211.137).
Specifically, the draft guidance states
certain circumstances under which we
intend to exercise enforcement
discretion and do not intend to take
action against repackagers for failure to
conduct stability studies to support
expiration dates for drug products in
accordance with FDA regulations.
The draft guidance is a proposed
revision of section 480.200 of the CPG
(CPG 7132b.11), which we issued in
February 1984 and revised in March
1995. We originally issued CPG
7132b.11 because unit-dose packaging
systems had become widespread in
health care, and questions had arisen as
to whether drugs that were repackaged
into unit-dose containers needed
expiration dates based on stability data
on the drugs in the unit-dose containers.
The CGMP regulations require that
each drug product bear an expiration
date derived from tests conducted on
samples stored in the immediate
container closure system in which the
drug is marketed (see § 211.137(a),
§ 211.166(a)(4) (21 CFR 211.166(a)(4))).
This expiration dating ensures the
drugs’ safety and efficacy over their
intended shelf life. CPG 7132b.11 notes
that the USP contains standards on
beyond-use dating of nonsterile solid
and liquid unit-dose drug products.
Since its adoption in 1984, the CPG
has stated that, in light of the USP
standards and under certain conditions,
the agency does not deem it necessary
that stability studies be conducted on
drugs that are repackaged into unit-dose
containers. Therefore, the CPG has
stated that we do not intend to initiate
enforcement action against any unitdose repackaging firm for failure to have
stability studies supporting expiration
dates, provided certain conditions are
met, including that the expiration date
does not exceed 6 months. At the time
the CPG was adopted, this
recommendation was substantially
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
30953
comparable to the USP standards on
expiration dating of nonsterile unit-dose
repackaged drug products.
In 2000, the USP revised its standards
on the beyond-use dating of nonsterile
solid and liquid dosage forms that are
packaged in single-unit and unit-dose
containers. The USP now states that, for
such products, the beyond-use date
must be 1 year from the date the drug
is packaged into the single-unit or unitdose container or the expiration date on
the manufacturer’s container, whichever
is earlier, unless stability data or the
manufacturer’s labeling indicates
otherwise (USP 27, General Notices and
Requirements, at 11).
We have considered the USP revision
to its beyond-use standard and believe
that similar conditions are appropriate
for CPG 7132b.11 for expiration dating.
We believe that under certain specified
conditions, it may be appropriate to
assign up to a one-year expiration dating
period to solid and liquid oral dosage
form drug products repackaged into
unit-dose containers, without
conducting new stability studies on the
repackaged drug products. Therefore,
we are proposing to revise CPG
7132b.11 to clarify the agency’s exercise
of enforcement discretion concerning
expiration dating of nonsterile solid and
liquid oral dosage form drug products
that are repackaged into unit-dose
containers.
Under draft revised CPG 7132b.11, the
expiration date for a nonsterile
repackaged unit-dose drug would not
exceed the following: (1) One year from
the date of repackaging, or (2) the
expiration date on the container of the
original manufacturer’s product,
whichever is earlier, unless stability
data or the original manufacturer’s
product labeling indicated otherwise,
and provided certain other
recommendations specified in CPG
7132b.11 were met. These other
conditions include, but are not limited
to, standards for containers, repackaging
operations, and the repackaging
environment.
Additionally, because CPG 7132b.11
serves as Attachment B to section
430.100 of the CPG (CPG 7132b.10,
‘‘Unit Dose Labeling for Solid and
Liquid Oral Dosage Forms’’), the
proposed revision of CPG 7132b.11 will
serve as Attachment B to CPG 7132b.10
when CPG 7132b.11 is finalized.
We invite comments on the draft
guidance. Additionally, we intend to
conduct further study of the
appropriateness of the proposed
revision of CPG 7132b.11 regarding
expiration dating on the unit-dose
containers of nonsterile repackaged
solid and liquid oral dosage form drug
E:\FR\FM\31MYN1.SGM
31MYN1
]]>Agencies
[Federal Register Volume 70, Number 103 (Tuesday, May 31, 2005)]
[Notices]
[Pages 30951-30953]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-10703]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 2005N-0178]
Agency Information Collection Activities; Proposed Collection;
Comment Request; Regulations Under the Federal Import Milk Act
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing an
opportunity for public comment on the proposed collection of certain
information by the agency. Under the Paperwork Reduction Act of 1995
(the PRA), Federal agencies are required to publish notice in the
Federal Register concerning each proposed collection of information,
including each proposed extension of an existing collection of
information, and to allow 60 days for public comment in response to the
notice. This notice solicits comments on reporting and recordkeeping
requirements in implementing the Federal Import Milk Act (FIMA).
DATES: Submit written or electronic comments on the collection of
information by August 1, 2005.
ADDRESSES: Submit electronic comments on the collection of information
to: https://www.fda.gov/dockets/ecomments. Submit written comments on
the collection of information to the Division of Dockets Management
(HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061,
Rockville, MD 20852. All comments should be identified with the docket
number found in brackets in the heading of this document.
FOR FURTHER INFORMATION CONTACT: Peggy Robbins, Office of Management
Programs (HFA-250), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-827-1223.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of
[[Page 30952]]
information they conduct or sponsor. ``Collection of information'' is
defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and includes agency
requests or requirements that members of the public submit reports,
keep records, or provide information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60-day notice in the Federal Register concerning
each proposed collection of information, including each proposed
extension of an existing collection of information, before submitting
the collection to OMB for approval. To comply with this requirement,
FDA is publishing notice of the proposed collection of information set
forth in this document.
With respect to the following collection of information, FDA
invites comments on these topics: (1) Whether the proposed collection
of information is necessary for the proper performance of FDA's
functions, including whether the information will have practical
utility; (2) the accuracy of FDA's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used; (3) ways to enhance the quality,
utility, and clarity of the information to be collected; and (4) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques, when
appropriate, and other forms of information technology.
Regulations Under the Federal Import Milk Act--21 CFR Part 1210 (OMB
Control Number 0910-0212)--Extension
Under the regulations implementing FIMA (21 U.S.C. 141-149), milk
or cream may be imported into the United States only by the holder of a
valid import milk permit. Before such permit is issued: (1) All cows
from which import milk or cream is produced must be physically examined
and found healthy; (2) if the milk or cream is imported raw, all such
cows must pass a tuberculin test; (3) the dairy farm and each plant in
which the milk or cream is processed or handled must be inspected and
found to meet certain sanitary requirements; (4) bacterial counts of
the milk at the time of importation must not exceed specified limits;
and (5) the temperature of the milk or cream at time of importation
must not exceed 50[deg] F. In addition, the regulations in part 1210
(21 CFR part 1210) require that dairy farmers and plants maintain
pasteurization records (Sec. 1210.15) and that each container of milk
or cream imported into the United States bear a tag with the product
type, permit number, and shipper's name and address (Sec. 1210.22).
FDA estimates the burden of this collection of information as
follows:
Table 1.--Estimated Annual Reporting Burden\1\
----------------------------------------------------------------------------------------------------------------
Annual
Form No. 21 CFR No. of Frequencyper Total Annual Hours per Total Hours
Section Respondents Response Responses Response
----------------------------------------------------------------------------------------------------------------
FDA 1815/Permits 1210.23 8 1 8 0.5 4.0
granted on
certificates
----------------------------------------------------------------------------------------------------------------
FDA 1993/ 1210.20 8 1 8 0.5 4.0
Application of
permit
----------------------------------------------------------------------------------------------------------------
FDA 1994/ 1210.13 1 1 1 0.5 0.5
Tuberculin test
----------------------------------------------------------------------------------------------------------------
FDA 1995/ 1210.12 1 1 1 0.5 0.5
Physical
examination of
cows
----------------------------------------------------------------------------------------------------------------
FDA 1996/ 1210.11 8 200 1,600 1.5 2,400
Sanitary
inspection of
dairy farms
----------------------------------------------------------------------------------------------------------------
FDA 1997/ 1210.14 8 1 8 2.0 16.0
Sanitary
inspections of
plants
----------------------------------------------------------------------------------------------------------------
Total .............. .............. .............. .............. .............. 2,425.0
----------------------------------------------------------------------------------------------------------------
\1\There are no capital costs or operating and maintenance costs associated with this collection of information.
Table 2.--Estimated Annual Recordkeeping Burden\1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
No. of Annual Frequency per
21 CFR Section Recordkeepers Recordkeeping Total Annual Records Hours per Record Total Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
1210.15 8 1 8 0.05 0.40
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\There are no capital costs or operating and maintenance costs associated with this collection of information.
These estimates are based on the number of current permit holders
and the number of inquiries that FDA has received regarding requests
for applications in the past 3 years. No burden has been estimated for
the tagging requirement in Sec. 1210.22 because the information on the
tag is either supplied by FDA (permit number) or is disclosed to third
parties as a usual and customary part of the shipper's normal business
activities (type of product, shipper's name and address). Under 5 CFR
1320.3(c)(2), the public disclosure of information originally supplied
by the Federal Government to the recipient for the purpose of
disclosure to the public is not a collection of information. Under 5
CFR 1320.3(b)(2)), the time, effort, and financial resources necessary
to comply with a collection of information are excluded from the burden
estimate if the reporting, recordkeeping, or disclosure activities
needed to comply are usual and customary because they would occur in
the normal course of activities. Low burden has been estimated for
Forms FDA 1994 and 1995 because they are not are not used often.
[[Page 30953]]
The Secretary of Health and Human Services has the discretion to allow
Form FDA 1815, a duly certified statement signed by an accredited
official of a foreign government, to be submitted in lieu of Forms FDA
1994 and 1995. To date, Form FDA 1815 has been submitted in lieu of
these forms.
Dated: May 17, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05-10703 Filed 5-27-05; 8:45 am]
BILLING CODE 4160-01-S
