[Federal Register Volume 82, Number 126 (Monday, July 3, 2017)]
[Notices]
[Pages 30875-30876]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-13890]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2016-N-2976; FDA-2016-N-3535; FDA-2013-N-1089; FDA-
2013-N-1619; FDA-2013-N-0719; FDA-2016-N-3586; FDA-2013-N-0796; FDA-
2016-N-0736; FDA-2016-N-3995; FDA-2013-D-0575; FDA-2016-N-0735]
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, 10A63, 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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Request for Information From U.S. 0910-0320 5/31/2020
Processors That Export to the European
Community..............................
Guidance for Industry: Special Protocol 0910-0470 5/31/2020
Assessment.............................
Use of Symbols on Labels and in Labeling 0910-0553 5/31/2020
of In Vitro Diagnostic Devices Intended
for Professional Use...................
Current Good Manufacturing Practice in 0910-0606 5/31/2020
Manufacturing, Packaging, Labeling, or
Holding Operations for Dietary
Supplements............................
Guidance for Industry: Planning for the 0910-0675 5/31/2020
Effects of High Absenteeism to Ensure
Availability of Medically Necessary
Drug Products..........................
[[Page 30876]]
Focus Groups About Drug Products as Used 0910-0677 5/31/2020
by the Food and Drug Administration....
Testing Communication on Medical Devices 0910-0678 5/31/2020
and Radiation-Emitting Products........
Tracking Network for PETNet, 0910-0680 5/31/2020
LivestockNet, and SampleNet............
Medical Devices: Pediatric Uses of 0910-0748 5/31/2020
Devices; Requirements for Submission of
Information on Pediatric Subpopulations
That Suffer From a Disease or Condition
That a Device is Intended to Treat,
Diagnose, or Cure......................
Guidance for Industry: Expedited 0910-0765 5/31/2020
Programs for Serious Conditions--Drugs
and Biologics..........................
Superimposed Text in Direct-to-Consumer 0910-0831 5/31/2020
Promotion of Prescription Drugs........
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Dated: June 27, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2017-13890 Filed 6-30-17; 8:45 am]
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