Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Food and Drug Administration's Research and Evaluation Survey for the Public Education Campaign on Tobacco Among LGBT (RESPECT), 10256 [2016-04277]
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Federal Register / Vol. 81, No. 39 / Monday, February 29, 2016 / Notices
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Dated: February 23, 2016.
Leslie Kux,
Associate Commissioner for Policy.
Dated: February 23, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016–04277 Filed 2–26–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2016–04223 Filed 2–26–16; 8:45 am]
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Food and Drug Administration
[Docket No. FDA–2016–N–0586]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Draft Food and Drug Administration
Tribal Consultation Policy; Availability;
Request for Comments
[Docket No. FDA–2015–N–2126]
AGENCY:
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Food and Drug Administration’s
Research and Evaluation Survey for
the Public Education Campaign on
Tobacco Among LGBT (RESPECT)
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Food and Drug Administration’s
Research and Evaluation Survey for the
Public Education Campaign on Tobacco
among LGBT (RESPECT)’’ has 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, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION: On
January 26, 2016, the Agency submitted
a proposed collection of information
entitled ‘‘Food and Drug
Administration’s Research and
Evaluation Survey for the Public
Education Campaign on Tobacco among
LGBT (RESPECT)’’ to OMB for review
and clearance under 44 U.S.C. 3507. 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. OMB has now approved the
information collection and has assigned
OMB control number 0910–0808. The
approval expires on January 31, 2019. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.reginfo.gov/
public/do/PRAMain.
April 4, 2016
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SUMMARY:
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19:23 Feb 26, 2016
Jkt 238001
Food and Drug Administration,
HHS.
Notice of availability; request
for comments.
ACTION:
The Food and Drug
Administration (FDA or we) is
announcing the availability of the draft
FDA Tribal Consultation Policy. We are
also announcing the establishment of a
docket to receive comments on the draft
FDA Tribal Consultation Policy. The
purpose of the FDA Tribal Consultation
Policy, when finalized, is to establish
clear policies to further the governmentto-government relationship between
FDA and American Indian and Alaskan
Native Tribes (hereafter, Indian Tribes)
and facilitate tribal consultation with
FDA. The draft FDA Tribal Consultation
Policy provides background on FDA’s
mission and organizational structure
and sets out principles and guidelines
for the tribal consultation process.
DATES: Comments must be received on
or before May 31, 2016.
ADDRESSES: You may submit comments
as follows:
SUMMARY:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
PO 00000
Frm 00052
Fmt 4703
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comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Division of
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Division of Dockets
Management, FDA will post your
comment, as well as any attachments,
except for information submitted,
marked and identified, as confidential,
if submitted as detailed in
‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2016–N–0586 for ‘‘Draft FDA Tribal
Consultation Policy; Availability;
Request for Comments.’’ Received
comments will be placed in the docket
and, except for those submitted as
‘‘Confidential Submissions,’’ publicly
viewable at https://www.regulations.gov
or at the Division of Dockets
Management between 9 a.m. and 4 p.m.,
Monday through Friday.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on
https://www.regulations.gov. Submit
both copies to the Division of Dockets
Management. If you do not wish your
name and contact information to be
made publicly available, you can
provide this information on the cover
sheet and not in the body of your
comments and you must identify this
information as ‘‘confidential.’’ Any
information marked as ‘‘confidential’’
will not be disclosed except in
accordance with 21 CFR 10.20 and other
applicable disclosure law. For more
E:\FR\FM\29FEN1.SGM
29FEN1
Agencies
[Federal Register Volume 81, Number 39 (Monday, February 29, 2016)]
[Notices]
[Page 10256]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-04277]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2015-N-2126]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approval; Food and Drug Administration's
Research and Evaluation Survey for the Public Education Campaign on
Tobacco Among LGBT (RESPECT)
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that a
collection of information entitled ``Food and Drug Administration's
Research and Evaluation Survey for the Public Education Campaign on
Tobacco among LGBT (RESPECT)'' has 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, 8455 Colesville Rd., COLE-14526, Silver
Spring, MD 20993-0002, PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: On January 26, 2016, the Agency submitted a
proposed collection of information entitled ``Food and Drug
Administration's Research and Evaluation Survey for the Public
Education Campaign on Tobacco among LGBT (RESPECT)'' to OMB for review
and clearance under 44 U.S.C. 3507. 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.
OMB has now approved the information collection and has assigned OMB
control number 0910-0808. The approval expires on January 31, 2019. A
copy of the supporting statement for this information collection is
available on the Internet at https://www.reginfo.gov/public/do/PRAMain.
April 4, 2016
Dated: February 23, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016-04277 Filed 2-26-16; 8:45 am]
BILLING CODE 4164-01-P