[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]


-----------------------------------------------------------------------

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.

-----------------------------------------------------------------------

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
------------------------------------------------------------------------
                                            OMB control    Date approval
           Title of collection                  No.           expires
------------------------------------------------------------------------
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................................
------------------------------------------------------------------------


    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


