[Federal Register Volume 83, Number 68 (Monday, April 9, 2018)]
[Notices]
[Pages 15152-15153]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-07146]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2014-N-0075; FDA-2011-N-0015; FDA-2011-N-0076; FDA-
2017-N-0932; FDA-2016-N-4487; FDA-2014-N-0345; FDA-2013-N-0523; FDA-
2017-N-2428; FDA-2008-N-0312; and FDA-2014-N-1072]
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
https://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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Good Laboratory Practice Regulations for 0910-0119 1/31/2021
Nonclinical Studies....................
Orphan Drug Designation Request Form and 0910-0167 1/31/2021
The Common European Medicines Agency/
Food and Drug Administration Form for
Orphan Medicinal Product Designation...
Electronic Records: Electronic 0910-0303 1/31/2021
Signatures.............................
Experimental Study on Warning Statements 0910-0848 1/31/2021
for Cigarette Graphic Health Warnings..
[[Page 15153]]
Consumer and Healthcare Professional 0910-0849 1/31/2021
Identification of and Responses to
Deceptive Prescription Drug Promotion..
Data to Support Drug Product 0910-0695 2/28/2021
Communications.........................
Applications for FDA Approval to Market 0910-0001 3/31/2021
a New Drug.............................
Animal Drug Adverse Event Reporting and 0910-0284 3/31/2021
Recordkeeping..........................
Extralabel Drug Use in Animals.......... 0910-0325 3/31/2021
Application for Participation in FDA 0910-0780 3/31/2021
Fellowship Programs....................
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Dated: April 3, 2018.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2018-07146 Filed 4-6-18; 8:45 am]
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