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Notice: Agency Information Collection Activities; Submission for Office
of Management and Budget Review; Comment Request; Exports: Notification
and Recordkeeping Requirements
Federal Register: May 8, 2008 (Volume 73, Number 90)
Page 26119
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
proposed collection of information has been submitted to the Office of
Management and Budget (OMB) for review and clearance under the
Paperwork Reduction Act of 1995.
DATES: Fax written comments on the collection of information by June 9,
2008.
ADDRESSES: To ensure that comments on the information collection are
received, OMB recommends that written comments be faxed to the Office
of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer,
FAX: 202-395-6974, or e-mailed to baguilar@omb.eop.gov. All comments
should be identified with the OMB control number 0910-0482. Also
include the FDA docket number found in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT: Jonna Capezzuto, Office of the Chief
Information Officer (HFA-250), Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857, 301-827-4659.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has
submitted the following proposed collection of information to OMB for
review and clearance.
Exports: Notification and Recordkeeping Requirements--(OMB Control
Number 0910-0482)--Extension
The respondents to this information collection are exporters who
have notified FDA of their intent to export unapproved products that
may not be sold or marketed in the United States as allowed under
section 801(e) of the Federal Food, Drug, and Cosmetic Act (the act)
(21 U.S.C. 381(e)). In general, the notification identifies the product
being exported (e.g. name, description, and in some cases, country of
destination) and specifies where the notification should be sent. These
notifications are sent only for an initial export; subsequent exports
of the same product to the same destination (or, in the case of certain
countries identified in section 802(b) of the act (21 U.S.C. 382(b)),
to any of those countries would not result in a notification to FDA.
The recordkeepers to this information collection are exporters who
export human drugs, biologics, devices, animal drugs, foods and
cosmetics that may not be sold in the United States to maintain records
demonstrating their compliance with the requirements in section
801(e)(1) of the act.
The total burden estimate of 39,120 is based on the number of
notifications received by the relevant FDA centers in fiscal year 2007,
or the last year the figures were available.
In the Federal Register of January 28, 2008 (73 FR 4874), FDA
published a 60-day notice requesting public comment on the information
collection provisions. No comments were received.
Table 1.--Estimated Annual Reporting Burden\1\
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No. of Annual Frequency Total Annual Hours per
21 CFR Section Respondents per Response Responses Response Total Hours
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1.101(d) and (e) 400 3 1,200 15 18,000
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\1\ There are no capital costs or operating and maintenance costs associated with this collection of
information.
Table 2.--Estimated Annual Recordkeeping Burden\1\
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Annual Frequency
21 CFR Section No. of per Total Annual Hours per Record Total Hours
Recordkeepers Recordkeeping Records
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1.101(b) and (c) 320 3 960 22 21,120
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\1\ There are no capital costs or operating and maintenance costs associated with this collection of
information.
Dated: May 1, 2008.
Jeffrey Shuren,
Associate Commissioner for Policy and Planning.
[FR Doc. E8-10204 Filed 5-7-08; 8:45 am]
BILLING CODE 4160-01-S
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