2020-20332. Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals  

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    AGENCY:

    Food and Drug Administration, Health and Human Services (HHS).

    ACTION:

    Notice.

    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.

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    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.

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    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

    Title of collectionOMB control No.Date approval expires
    Reporting and Recordkeeping for Electronic Products—General Requirements0910-00258/31/2023
    Current Good Manufacturing Practice Regulations for Medicated Feed0910-01528/31/2023
    Good Manufacturing Practice Regulations for Type A Medicated Articles, 21 CFR Part 2260910-01548/31/2023
    Food Labeling Regulations0910-03818/31/2023
    Prior Notice of Imported Food Under the Public Health Security and Bioterrorism Preparedness and Response Act of 20020910-05208/31/2020
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    Animal Drug User Fee Program0910-05408/31/2023
    Index of Legally Marketed Unapproved New Animal Drugs for Minor Species0910-06208/31/2023
    Potential Tobacco Product Violations Reporting Form0910-07168/31/2023
    Donor Risk Assessment Questionnaire for the FDA/National Heart, Lung, and Blood Institute—Sponsored Transfusion-Transmissible Infections Monitoring System—Risk Factor Elicitation0910-08418/31/2023
    Generic Clearance for Qualitative Data to Support Social and Behavioral Research for Food, Dietary Supplements, Cosmetics, and Animal Food and Feed0910-08918/31/2023
    Health Care Providers Understanding of Opioid Analgesic Abuse-Deterrent Formulations: Phase 2 and 3 Surveys0910-08928/31/2023
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    Dated: September 9, 2020.

    Lowell J. Schiller,

    Principal Associate Commissioner for Policy.

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    [FR Doc. 2020-20332 Filed 9-14-20; 8:45 am]

    BILLING CODE 4164-01-P

Document Information

Published:
09/15/2020
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
2020-20332
Pages:
57220-57221 (2 pages)
Docket Numbers:
Docket Nos. FDA-2013-N-0618, FDA-2010-N-0601, FDA-2010-N-0598, FDA-2013-N-1155, FDA-2010-N-0118, FDA-2020-N-0145, FDA-2010-N-0597, FDA-2014-N-0086, FDA-2016-N-2836, FDA-2019-N-5841, and FDA-2019-N-5973
PDF File:
2020-20332.pdf
Supporting Documents:
» Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals
» Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Generic Clearance for Qualitative Data To Support Social and Behavioral Research for Food, Dietary Supplements, Cosmetics, and Animal Food and Feed
» Agency Information Collection Activities; Proposed Collection; Comment Request; Generic Clearance for Qualitative Data To Support Social and Behavioral Research for Food, Dietary Supplements, Cosmetics, and Animal Food and Feed