[Federal Register Volume 81, Number 132 (Monday, July 11, 2016)]
[Notices]
[Pages 44875-44876]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-16349]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2009-N-0221; FDA-2012-N-0559; FDA-2015-N-3287; FDA-
2015-N-3815; FDA-2007-D-0429; FDA-2012-N-0447; FDA-2011-D-0597; FDA-
2011-D-0164; FDA-2013-N-0013; FDA-2011-N-0146; FDA-2014-N-1533; FDA-
2011-N-0921; FDA-2015-N-2163]


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: FDA PRA Staff, Office of Operations, 
Food and Drug Administration, Three White Flint North 10A63, 11601 
Landsdown St., North Bethesda, MD 20852, [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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Food Labeling: Notification Procedures         0910-0331       6/30/2019
 for Statements on Dietary Supplements..
PHS Guideline on Infectious Disease            0910-0456       6/30/2019
 Issues in Xenotransplantation..........
MDUFMA Small Business Qualification            0910-0508       6/30/2019
 Certification..........................
Electronic Submission of Medical Device        0910-0625       6/30/2019
 Registration and Listing...............
Guidance for Industry on Q & A Regarding       0910-0641       6/30/2019
 Labeling of Nonprescription Human Drug
 Products Marketed Without an Approved
 Application as Required by the Dietary
 Supplement & Nonprescription Drug
 Consumer Protection Act................
Antimicrobial Animal Drug Distribution         0910-0659       6/30/2019
 Reports and Recordkeeping..............
Guidance for Industry on Oversight of          0910-0733       6/30/2019
 Clinical Investigations: A Risk-Based
 Approach to Monitoring.................
Guidance for Industry on Safety Labeling       0910-0734       6/30/2019
 Changes; Implementation of the Federal
 Food, Drug, and Cosmetic Act...........
Accreditation of Third Party                   0910-0750       6/30/2019
 Certification Bodies to Conduct Food
 Safety Audits and Issue Certifications.
Sanitary Transportation of Human and           0910-0773       6/30/2019
 Animal Food............................
National Panel of Tobacco Consumer             0910-0815       6/30/2019
 Studies................................
Standards for the Growing, Harvesting,         0910-0816       6/30/2019
 Packaging, and Holding of Produce for
 Human Consumption......................
Hearing, Aging, and Direct-to-Consumer         0910-0818       6/30/2019
 Television Advertisements..............
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    Dated: July 6, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016-16349 Filed 7-8-16; 8:45 am]
 BILLING CODE 4164-01-P