[Federal Register Volume 81, Number 243 (Monday, December 19, 2016)]
[Notices]
[Pages 91939-91940]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-30351]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2012-N-0873; FDA-2008-D-0031; FDA-2013-N-0242; FDA-
2013-N-0125; FDA-2013-N-0093; FDA-2016-N-1593; FDA-2015-N-2406; FDA-
2013-N-0450; FDA-2011-N-0830]


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: FDA PRA Staff, Office of Operations, 
Food and Drug Administration, Three White Flint North, 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
------------------------------------------------------------------------
                                            OMB control    Date approval
           Title of collection                  No.           expires
------------------------------------------------------------------------
Bar Code Label Requirements for Human          0910-0537       9/30/2019
 Drug Products and Biological Products..
Clinical Laboratory Improvement                0910-0598       9/30/2019
 Amendments Waiver Applications.........
Current Good Manufacturing Practices for       0910-0667       9/30/2019
 Positron Emission Tomography Drugs.....
Medical Devices: Use of Certain Symbols        0910-0740       9/30/2019
 in Labeling--Glossary to Support the
 Use of Symbols in Labeling.............
Evaluation of the Program for Enhanced         0910-0746       9/30/2019
 Review Transparency and Communication
 for New Molecular Entity New Drug
 Applications and Original Biologics
 License Applications in Prescription
 Drug User Fee Act......................

[[Page 91940]]

 
Medical Device Accessories..............       0910-0823       9/30/2019
Market Claims in Direct-to-Consumer            0910-0824       9/30/2019
 Prescription Drug Print Ads............
Abbreviated New Animal Drug Applications       0910-0669      10/31/2019
Abbreviated New Drug Applications and          0910-0786      11/30/2019
 505(b)(2) Applications.................
------------------------------------------------------------------------


    Dated: December 13, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016-30351 Filed 12-16-16; 8:45 am]
 BILLING CODE 4164-01-P