[Federal Register Volume 62, Number 112 (Wednesday, June 11, 1997)]
[Notices]
[Pages 31830-31831]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-15168]
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 97N-0212]
Agency Information Collection Activities: Proposed Collection;
Comment Request; Extension
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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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 the electronic collection of
data by FDA regarding FDA-regulated products of foreign origin that are
being offered for import into the United States.
DATES: Submit written comments on the collection of information by
August 11, 1997.
ADDRESSES: Submit written comments on the collection of information to
the Dockets Management Branch (HFA-305), Food and Drug Administration,
12420 Parklawn Dr., rm. 1-23, Rockville, MD 20857. All comments should
be identified with the docket number found in brackets in the heading
of this document.
FOR FURTHER INFORMATION CONTACT: Margaret R. Wolff, Office of
Information Resources Management (HFA-250), Food and Drug
Administration, 5600 Fishers Lane, rm. 16B-19, 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 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 listed below.
With respect to the following collection of information, FDA
invites comments on: (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.
Importer's Entry Notice--(OMB Control Number 0910-0046)--Extension
Section 801 of the Federal Food, Drug, and Cosmetic Act (the act)
(21 U.S.C. 381) charges FDA with the following responsibilities: (1)
Assuring that foreign-origin FDA-regulated foods, drugs, cosmetics,
medical devices, and radiological health products offered for import
into the United States meet the same requirements of the act as do
domestic products; and (2) preventing shipments from entering the
country if they are not in compliance.
The information collected by FDA consists of the following: (1)
Product code, an alpha-numeric series of characters that identifies
each product FDA regulates; (2) FDA country of origin, the country
where the FDA-registered or FDA-responsible firm is located; (3) FDA
manufacturer, the party who manufactured, grew, assembled, or otherwise
processed the goods (if more than one, the last party who substantially
transformed the product); (4) shipper, the party responsible for
packing, consolidating, or arranging the shipment of the goods to their
final destination; (5) quantity and value of the shipment; and (6) if
appropriate, affirmation of compliance, a code that conveys specific
FDA information, such as registration number, foreign government
certification, etc. This information is collected electronically by the
entry filer via the U.S. Customs Service's Automated Commercial System
at the same time he/she files an entry for import with the U.S. Customs
Service. FDA uses the information to make admissibility decisions about
[[Page 31831]]
FDA-regulated products offered for import into the United States.
FDA estimates the burden of this collection of information as
follows:
Estimated Annual Reporting Burden
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Annual Frequency Total Annual
No. of Respondents per Response Responses Hours per Response Total Hours
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2,505 1,212.54 3,037,426 0.07 h 229,693
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There are no capital costs or operating and maintenance costs associated with this collection.
The source of the estimate for the number of respondents is the
number of importers who submitted entry data for foreign-origin FDA-
regulated products in 1996. The estimated reporting burden is based on
information obtained by contacting several past respondents.
Dated: June 3, 1997.
William K. Hubbard,
Associate Commissioner for Policy Coordination.
[FR Doc. 97-15168 Filed 6-10-97; 8:45 am]
BILLING CODE 4160-01-F
