[Federal Register Volume 83, Number 219 (Tuesday, November 13, 2018)]
[Notices]
[Page 56347]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-24609]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2017-N-0558; FDA-2017-N-1315; FDA-2011-N-0776; FDA-
2018-N-3038; FDA-2018-N-0405; FDA-2014-N-1048; FDA-2011-N-0908; FDA-
2011-N-0920; and FDA-2018-N-1857]
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 No. expires
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Disclosures in Professional and Consumer 0910-0860 9/30/2020
Prescription Drug Promotion............
Experimental Study of Risk Information 0910-0861 9/30/2020
Amount and Location in Direct-to-
Consumer Print Ads.....................
Reclassification Petitions for Medical 0910-0138 9/30/2021
Devices................................
Request for Samples and Protocols....... 0910-0206 9/30/2021
Medical Device Recall Authority......... 0910-0432 9/30/2021
Food Safety, Health, and Diet Survey.... 0910-0345 10/31/2020
Medical Device Labeling Regulations..... 0910-0485 10/30/2021
GFI: Clinical Trial Sponsors on the 0910-0581 10/31/2021
Establishment and Operation of Clinical
Trial Data Monitoring Committees.......
Current Good Manufacturing Practice and 0910-0751 10/31/2021
Hazard Analysis and Risk-Based
Preventive Controls for Human Food.....
Current Good Manufacturing Practice and 0910-0789 10/31/2021
Hazard Analysis and Risk-Based
Preventive Controls for Food for
Animals................................
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Dated: November 5, 2018.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2018-24609 Filed 11-9-18; 8:45 am]
BILLING CODE 4164-01-P