Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals, 62743 [2016-21877]

Download as PDF Federal Register / Vol. 81, No. 176 / Monday, September 12, 2016 / Notices ACTION: DEPARTMENT OF HEALTH AND HUMAN SERVICES 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, PRAStaff@ fda.hhs.gov. SUPPLEMENTARY INFORMATION: The following is a list of FDA information collections recently approved by OMB SUMMARY: Food and Drug Administration [Docket Nos. FDA–2016–N–0628; FDA–2012–N–0306; FDA–2002–N–0323; FDA–2012–N–0427; FDA–2012–N–0536; FDA–2012–N–0560; FDA–2015–N–3662; FDA–2012–N–0976; FDA–2013–N–0297; FDA–2012–N–1203; FDA–2011–D–0893; FDA–2014–N–0189; FDA–2012–N–1210] Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals AGENCY: Notice. Food and Drug Administration, HHS. 62743 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 No. Title of collection Reporting Associated with New Animal Drug Applications ..................................................................................... Administrative Detention and Banned Medical Devices ......................................................................................... Registration of Food Facilities ................................................................................................................................. Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002 ..................................................................................................................................................................... Medical Device User Fee Cover Sheet—FDA Form 3601 ..................................................................................... Guidance on Informed Consent for in Vitro Diagnostic Studies Using Leftover Human Specimens That Are Not Individually Identifiable ......................................................................................................................................... Guidance for Reagents for Detection of Specific Novel Influenza A Viruses ......................................................... Guidance: Emergency Use Authorization of Medical Products .............................................................................. Prevention of Salmonella Enteritidis in Shell Eggs During Production—Recordkeeping and Registration Provisions ..................................................................................................................................................................... Information to Accompany Humanitarian Device Exemption Applications and Annual Distribution Number Reporting Requirements ........................................................................................................................................... Guidance for Center for Devices and Radiological Health Appeals Processes ..................................................... Deeming Tobacco Products To Be Subject to the FD&C Act ................................................................................ Food Labeling: Revision of the Nutrition Facts Label and Supplement Facts Label ............................................. Dated: September 6, 2016. Leslie Kux, Associate Commissioner for Policy. DEPARTMENT OF HEALTH AND HUMAN SERVICES Advisory Committee, Office of Science, Center for Tobacco Products. FDA seeks to include the views of women and men, members of all racial and ethnic groups, and individuals with and without disabilities on its advisory committees and, therefore, encourages nominations of appropriately qualified candidates from these groups. Food and Drug Administration DATES: [FR Doc. 2016–21877 Filed 9–9–16; 8:45 am] BILLING CODE 4164–01–P Nominations received on or before November 14, 2016 will be given first consideration for membership on the Tobacco Products Scientific Advisory Committee. Nominations received after November 14, 2016 will be considered for nomination to the committee as later vacancies occur. [Docket No. FDA–2016–N–0001] sradovich on DSK3GMQ082PROD with NOTICES Request for Nominations for Voting Members on a Public Advisory Committee; Tobacco Products Scientific Advisory Committee AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is requesting nominations for voting members to serve on the Tobacco Products Scientific SUMMARY: VerDate Sep<11>2014 18:40 Sep 09, 2016 Jkt 238001 All nominations for membership should be sent electronically by logging into the FDA Advisory Nomination Portal: http:// www.accessdata.fda.gov/scripts/ FACTRSPortal/FACTRS/index.cfm or by mail to Advisory Committee Oversight and Management Staff, Food and Drug Administration, 10903 New Hampshire ADDRESSES: PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 Date approval expires 0910–0032 0910–0114 0910–0502 8/31/2019 8/31/2019 8/31/2019 0910–0510 0910–0511 8/31/2019 8/31/2019 0910–0582 0910–0584 0910–0595 8/31/2019 8/31/2019 8/31/2019 0910–0660 8/31/2019 0910–0661 0910–0738 0910–0768 0910–0813 8/31/2019 8/31/2019 8/31/2019 7/31/2019 Ave., Bldg. 32, Rm. 5103, Silver Spring, MD 20993–0002. FOR FURTHER INFORMATION CONTACT: Regarding all nomination questions for membership, the primary contact is: Caryn Cohen, Office of Science, Center for Tobacco Products, Food and Drug Administration, Document Control Center, 10903 New Hampshire Ave., Bldg. 71, Rm. G335, Silver Spring, MD 20993–0002, 1–877–287–1373 (choose Option 5), TPSAC@fda.hhs.gov. Information about becoming a member on an FDA advisory committee can also be obtained by visiting FDA’s Web site by using the following link: http://www.fda.gov/ AdvisoryCommittees/default.htm. SUPPLEMENTARY INFORMATION: FDA is requesting nominations for voting members on the Tobacco Products Scientific Advisory Committee. I. General Description of the Committee Duties The Tobacco Products Scientific Advisory Committee (the Committee) E:\FR\FM\12SEN1.SGM 12SEN1

Agencies

[Federal Register Volume 81, Number 176 (Monday, September 12, 2016)]
[Notices]
[Page 62743]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-21877]



[[Page 62743]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2016-N-0628; FDA-2012-N-0306; FDA-2002-N-0323; FDA-
2012-N-0427; FDA-2012-N-0536; FDA-2012-N-0560; FDA-2015-N-3662; FDA-
2012-N-0976; FDA-2013-N-0297; FDA-2012-N-1203; FDA-2011-D-0893; FDA-
2014-N-0189; FDA-2012-N-1210]


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, 11601 Landsdown 
St., North Bethesda, MD 20852, PRAStaff@fda.hhs.gov.

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
------------------------------------------------------------------------
Reporting Associated with New Animal           0910-0032       8/31/2019
 Drug Applications......................
Administrative Detention and Banned            0910-0114       8/31/2019
 Medical Devices........................
Registration of Food Facilities.........       0910-0502       8/31/2019
Inspection by Accredited Persons Program       0910-0510       8/31/2019
 Under the Medical Device User Fee and
 Modernization Act of 2002..............
Medical Device User Fee Cover Sheet--FDA       0910-0511       8/31/2019
 Form 3601..............................
Guidance on Informed Consent for in            0910-0582       8/31/2019
 Vitro Diagnostic Studies Using Leftover
 Human Specimens That Are Not
 Individually Identifiable..............
Guidance for Reagents for Detection of         0910-0584       8/31/2019
 Specific Novel Influenza A Viruses.....
Guidance: Emergency Use Authorization of       0910-0595       8/31/2019
 Medical Products.......................
Prevention of Salmonella Enteritidis in        0910-0660       8/31/2019
 Shell Eggs During Production--
 Recordkeeping and Registration
 Provisions.............................
Information to Accompany Humanitarian          0910-0661       8/31/2019
 Device Exemption Applications and
 Annual Distribution Number Reporting
 Requirements...........................
Guidance for Center for Devices and            0910-0738       8/31/2019
 Radiological Health Appeals Processes..
Deeming Tobacco Products To Be Subject         0910-0768       8/31/2019
 to the FD&C Act........................
Food Labeling: Revision of the Nutrition       0910-0813       7/31/2019
 Facts Label and Supplement Facts Label.
------------------------------------------------------------------------


    Dated: September 6, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016-21877 Filed 9-9-16; 8:45 am]
 BILLING CODE 4164-01-P