[Federal Register Volume 85, Number 20 (Thursday, January 30, 2020)]
[Notices]
[Pages 5446-5447]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-01655]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2018-N-3442; FDA-2013-N-0557; FDA-2013-N-0514; FDA-
2013-N-0190; FDA-2013-N-1428; FDA-2019-N-0075; FDA-2016-N-2544; FDA-
2019-N-2778; FDA-2012-N-0977; FDA-2013-N-0823; FDA-2009-N-0380; FDA-
2013-N-1147; FDA-2010-N-0117; FDA-2010-D-0350; FDA-2010-D-0319; FDA-
2012-D-0530; and FDA-2016-N-2683]
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,
[email protected].
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 http://www.reginfo.gov/public/do/PRAMain. 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 number expires
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Web-Based Pilot Survey to Assess Allergy 0910-0881 1/31/2021
to Cosmetics in the United States......
Postmarket Surveillance of Medical 0910-0449 11/30/2022
Devices................................
Administrative Procedures for Clinical 0910-0607 11/30/2022
Laboratory Improvement Amendments
Categorization.........................
[[Page 5447]]
Requirements Under the Comprehensive 0910-0671 11/30/2022
Smokeless Tobacco Health Education Act
of 1986, as Amended by the Family
Smoking Prevention and Tobacco Control
Act....................................
Electronic Drug Product Reporting for 0910-0827 11/30/2022
Human Drug Compounding Outsourcing
Facilities Under Section 503B of the
Federal Food, Drug, and Cosmetic Act...
Experimental Study on Measuring Consumer 0910-0880 11/30/2022
Comprehension of Displays of Harmful
and Potentially Harmful Constituents in
Tobacco Products and Tobacco Smoke.....
Medical Devices; Current Good 0910-0073 12/31/2022
Manufacturing Practice Quality System
Regulation.............................
Threshold of Regulation for Substances 0910-0298 12/31/2022
Used in Food-Contact Articles..........
Regulations Restricting the Sale and 0910-0312 12/31/2022
Distribution of Cigarettes and
Smokeless Tobacco to Protect Children
and Adolescents........................
Format and Content Requirements for Over- 0910-0340 12/31/2022
the-Counter Drug Product Labeling......
Product Jurisdiction: Assignment of 0910-0523 12/31/2022
Agency Component for Review of
Premarket Applications.................
Preparing a Claim of Categorical 0910-0541 12/31/2022
Exclusion or an Environmental
Assessment for Submission to the Center
for Food Safety and Applied Nutrition..
Hypertension Indication: Drug Labeling 0910-0670 12/31/2022
for Cardiovascular Outcome Claims......
Guidance for Tobacco Retailers on 0910-0745 12/31/2022
Tobacco Retailer Training Programs.....
Dear Health Care Provider Letters: 0910-0754 12/31/2022
Improving Communication of Important
Safety Information.....................
Requests for Feedback on Medical Device 0910-0756 12/31/2022
Submissions............................
Data to Support Social and Behavioral 0910-0847 12/31/2022
Research as Used by the Food and Drug
Administration.........................
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Dated: January 24, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-01655 Filed 1-29-20; 8:45 am]
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