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