[Federal Register Volume 85, Number 169 (Monday, August 31, 2020)]
[Notices]
[Pages 53822-53823]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-19092]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2019-N-3657; FDA-2019-N-6085; FDA-2017-N-6381; FDA-
2017-N-0084; FDA-2013-N-0731; FDA-2019-N-5971; FDA-2014-N-1021; and 
FDA-2019-N-3018]


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 
https://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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Accreditation Scheme for Conformity            0910-0889       6/30/2023
 Assessment Pilot Program...............
General Administrative Practice and            0910-0191       7/31/2023
 Procedures.............................
Records and Reports Concerning                 0910-0284       7/31/2023
 Experience With Approved New Animal
 Drugs..................................
Adverse Event Program for Medical              0910-0471       7/31/2023
 Devices (Medical Product Safety Network
Human Cells, Tissues, and Cellular and         0910-0543       7/31/2023
 Tissue-Based Products: Establishment
 Registration and Listing; Eligibility
 Determination for Donors; and Current
 Good Tissue Practice...................
Recommendations to Reduce the Risk of          0910-0681       7/31/2023
 Transfusion-Transmitted of Infection in
 Whole Blood and Blood Components;
 Agency Guidance........................
Food Labeling; Gluten-Free Labeling of         0910-0817       8/31/2023
 Fermented or Hydrolyzed Foods..........

[[Page 53823]]

 
Healthcare Provider Perception of Boxed        0910-0890       8/31/2023
 Warning Information Survey.............
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    Dated: August 24, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-19092 Filed 8-28-20; 8:45 am]
BILLING CODE 4164-01-P