[Federal Register Volume 81, Number 69 (Monday, April 11, 2016)]
[Notices]
[Pages 21355-21356]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-08153]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2012-N-0564, FDA-2015-N-0797, FDA-2012-N-0021, FDA-
2012-N-0280, FDA-2007-D-0372, FDA-2014-D-0044]
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, 8455 Colesville Rd., COLE-14526, Silver
Spring, MD 20993-0002, [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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Labeling of Dietary Supplements as 0910-0642 2/28/2019
Required by the Dietary Supplement and
Nonprescription Drug Consumer
Protection Act.........................
Foreign Supplier Verification Programs 0910-0752 2/28/2019
for Importers of Food for Humans and
Animals................................
Substances Generally Recognized as Safe: 0910-0342 3/31/2019
Notification Procedure.................
Financial Disclosure by Clinical 0910-0396 3/31/2019
Investigators..........................
Adverse Event Reporting and 0910-0635 3/31/2019
Recordkeeping for Dietary Supplements
as Required by the Dietary Supplement
and Nonprescription Drug Consumer
Protection Act.........................
Exempt Infant Formula Production: 0910-0811 3/31/2019
Current Good Manufacturing Practices
(CGMPs), Quality Control Procedures,
Conduct of Audits, and Records.........
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[[Page 21356]]
Dated: April 5, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016-08153 Filed 4-8-16; 8:45 am]
BILLING CODE 4164-01-P