Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals, 56031 [2017-25452]
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56031
Federal Register / Vol. 82, No. 226 / Monday, November 27, 2017 / Notices
Estimated Total/Annual Burden
Hours: 244.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 330
C Street SW., Washington, DC 20201,
Attn: OPRE Reports Clearance Officer.
All requests should be identified by the
title of the information collection. Email
address: OPREinfocollection@
acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Email: OIRA_
SUBMISSION@OMB.EOP.GOV, Attn:
Desk Officer for the Administration for
Children and Families.
Mary Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2017–25444 Filed 11–24–17; 8:45 am]
BILLING CODE 4184–37–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA–2010–N–0601, FDA–
2010–N–0598, FDA–2010–N–0600, FDA–
2007–N–0037, FDA–2010–N–0597, FDA–
2011–N–0017, and FDA–2016–N–2496]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approvals
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is publishing a
list of information collections that have
SUMMARY:
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, 10A–12M, 11601
Landsdown St., North Bethesda, MD
20852, 301–796–7726, PRAStaff@
fda.hhs.gov.
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.
SUPPLEMENTARY INFORMATION:
TABLE 1—LIST OF INFORMATION COLLECTIONS APPROVED BY OMB
OMB
control No.
Title of collection
Current Good Manufacturing Practice for Medicated Feeds ......................................................................
Current Good Manufacturing Practice for Type A Medicated Articles ........................................................
Animal Drug User Fee Cover Sheet, Form FDA 3546 ...............................................................................
Animal Drug User Fee Waivers and Reductions ........................................................................................
Index of Legally Marketed Unappropriated New Animal Drugs for Minor Species ....................................
Voluntary National Retail Food Regulatory Program Standards ................................................................
Impact Trade Auxiliary Communication System .........................................................................................
Dated: November 20, 2017.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2017–25452 Filed 11–24–17; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
asabaliauskas on DSKBBXCHB2PROD with NOTICES
[Docket No. FDA–2010–N–0161]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Export of Food and
Drug Administration-Regulated
Products: Export Certificates
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
announcing an opportunity for public
SUMMARY:
VerDate Sep<11>2014
16:59 Nov 24, 2017
Jkt 244001
comment on the proposed collection of
certain information by the Agency.
Under the Paperwork Reduction Act of
1995 (PRA), Federal Agencies are
required to publish notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information, and
to allow 60 days for public comment in
response to the notice. This notice
solicits comments on export certificates
for the export of FDA-regulated
products.
Submit either electronic or
written comments on the collection of
information by January 26, 2018.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. Electronic comments must
be submitted on or before January 26,
2018. The https://www.regulations.gov
electronic filing system will accept
comments until midnight Eastern Time
DATES:
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
0910–0152
0910–0154
0910–0539
0910–0540
0910–0620
0910–0621
0910–0842
Date
approval
expires
8/31/2020
8/31/2020
8/31/2020
8/31/2020
8/31/2020
8/31/2020
8/31/2020
at the end of January 26, 2018.
Comments received by mail/hand
delivery/courier (for written/paper
submissions) will be considered timely
if they are postmarked or the delivery
service acceptance receipt is on or
before that date.
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
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]]>Agencies
[Federal Register Volume 82, Number 226 (Monday, November 27, 2017)]
[Notices]
[Page 56031]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-25452]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2010-N-0601, FDA-2010-N-0598, FDA-2010-N-0600, FDA-
2007-N-0037, FDA-2010-N-0597, FDA-2011-N-0017, and FDA-2016-N-2496]
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: Ila S. Mizrachi, Office of Operations,
Food and Drug Administration, Three White Flint North, 10A-12M, 11601
Landsdown St., North Bethesda, MD 20852, 301-796-7726,
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
------------------------------------------------------------------------
Date approval
Title of collection OMB control No. expires
------------------------------------------------------------------------
Current Good Manufacturing 0910-0152 8/31/2020
Practice for Medicated Feeds.....
Current Good Manufacturing 0910-0154 8/31/2020
Practice for Type A Medicated
Articles.........................
Animal Drug User Fee Cover Sheet, 0910-0539 8/31/2020
Form FDA 3546....................
Animal Drug User Fee Waivers and 0910-0540 8/31/2020
Reductions.......................
Index of Legally Marketed 0910-0620 8/31/2020
Unappropriated New Animal Drugs
for Minor Species................
Voluntary National Retail Food 0910-0621 8/31/2020
Regulatory Program Standards.....
Impact Trade Auxiliary 0910-0842 8/31/2020
Communication System.............
------------------------------------------------------------------------
Dated: November 20, 2017.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2017-25452 Filed 11-24-17; 8:45 am]
BILLING CODE 4164-01-P
