[Federal Register Volume 85, Number 52 (Tuesday, March 17, 2020)]
[Notices]
[Pages 15187-15188]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-05354]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2019-N-3077; FDA-2013-N-0403; FDA-2013-N-0579; FDA-
2016-N-2474; FDA-2013-N-0717; FDA-2018-N-3728; FDA-2013-N-0797; FDA-
2013-N-0578; FDA-2013-N-0879; FDA-2012-N-0197; FDA-2016-N-3586; FDA-
2016-N-4319; and FDA-2013-N-0764]


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, 
PRAStaff@fda.hhs.gov.

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                  No.           expires
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Obtaining Information to Understand            0910-0883       1/31/2021
 Challenges and Opportunities
 Encountered by Compounding Outsourcing
 Facilities.............................
Protection of Human Subjects; Informed         0910-0130       1/31/2023
 Consent; and Institutional Boards......
Biological Products: Reporting and             0910-0458       1/31/2023
 Biological Product Deviations and Human
 Cells, Tissues, and Cellular and Tissue-
 Based Deviations in Manufacturing......
Reporting Associated with Designated New       0910-0605       1/31/2023
 Animal Drugs for Minor Use and Minor
 Species................................
Evaluation of the Food and Drug                0910-0753       1/31/2023
 Administration's General Market Youth
 Tobacco Prevention Campaign............
Collection of Conflict of Interest             0910-0882       1/31/2023
 Information for Participation in Food
 and Drug Administration Non-Employee
 Fellowship and Traineeship Programs....
Human Tissue Intended for                      0910-0302       2/28/2023
 Transplantation........................
General Licensing Provisions: Biologics        0910-0338       2/28/2023
 License Application, Changes to an
 Approved Application, Labeling,
 Revocation and Suspension,
 Postmarketing Studies Status Reports,
 and Form FDA 356h......................
Procedures for the Safe Processing and         0910-0354       2/28/2023
 Importing of Fish and Fishery Products.
Medical Devices; Shortages Data                0910-0491       2/28/2023
 Collection System......................
Focus Groups About Drug Products as Used       0910-0677       2/28/2023
 by the Food and Drug Administration....

[[Page 15188]]

 
Unique Device Identification System.....       0910-0720       2/28/2023
Animal Feed Regulatory Program Standards       0910-0760       2/28/2023
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    Dated: March 11, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-05354 Filed 3-16-20; 8:45 am]
 BILLING CODE 4164-01-P


