Notice2022-01692
Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
Primary source
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Published
January 28, 2022
Issuing agencies
Health and Human Services DepartmentFood and Drug Administration
Abstract
The Food and Drug Administration (FDA) is publishing a list of information collections that have been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
Full Text
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<title>Federal Register, Volume 87 Issue 19 (Friday, January 28, 2022)</title>
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[Federal Register Volume 87, Number 19 (Friday, January 28, 2022)]
[Notices]
[Page 4628]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2022-01692]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2011-N-0742; FDA-2018-N-0180; FDA-2019-N-2854; FDA-
2021-N-0515; FDA-2014-N-1960; FDA-2017-D-6069; and FDA-2019-N-3325]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is publishing a list of
information collections that have been approved by the Office of
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, Office of Operations,
Food and Drug Administration, Three White Flint North, 10A-12M, 11601
Landsdown St., North Bethesda, MD 20852, 301-796-7726,
<a href="/cdn-cgi/l/email-protection#6a3a382b391e0b0c0c2a0c0e0b44020219440d051c"><span class="__cf_email__" data-cfemail="4e1e1c0f1d3a2f28280e282a2f6026263d60292138">[email protected]</span></a>.
SUPPLEMENTARY INFORMATION: The following is a list of FDA information
collections recently approved by OMB under section 3507 of the
Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control
number and expiration date of OMB approval for each information
collection are shown in table 1. Copies of the supporting statements
for the information collections are available on the internet at
<a href="https://www.reginfo.gov/public/do/PRAMain">https://www.reginfo.gov/public/do/PRAMain</a>. An Agency may not conduct or
sponsor, and a person is not required to respond to, a collection of
information unless it displays a currently valid OMB control number.
Table 1--List of Information Collections Approved by OMB
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OMB control Date approval
Title of collection No. expires
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Registration of Producers of Drugs and 0910-0045 12/31/2024
Listing of Drugs in Commercial
Distribution...........................
Generic Clearance for the Collection of 0910-0810 12/31/2024
Qualitative Data on Tobacco Products
and Communications.....................
Premarket Tobacco Product Applications 0910-0879 12/31/2024
and Recordkeeping Requirements.........
Postmarketing Adverse Experience 0910-0230 1/31/2025
Reporting and Recordkeeping............
MedWatch: Adverse Event and Product 0910-0291 1/31/2025
Experience Reporting System (Paper
Based).................................
De Novo Classification Process 0910-0844 1/31/2025
(Evaluation of Automatic Class III
Designation)...........................
Laboratory Accreditation for Analyses of 0910-0898 1/31/2025
Foods..................................
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Dated: January 20, 2022.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2022-01692 Filed 1-27-22; 8:45 am]
BILLING CODE 4164-01-P
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