Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals, 71925 [2020-25022]
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Federal Register / Vol. 85, No. 219 / Thursday, November 12, 2020 / Notices
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.
SUMMARY:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA–2020–N–0908; FDA–
2010–N–0583; FDA–2020–N–0257; FDA–
2008–N–0490; FDA–2011–N–0017; FDA–
2011–N–0144; FDA–2015–D–3327; FDA–
2020–N–1207]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approvals
AGENCY:
Food and Drug Administration,
The
following is a list of FDA information
collections recently approved by OMB
SUPPLEMENTARY INFORMATION:
HHS.
ACTION:
Notice.
71925
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
Submission of Petitions: Food Additive, Color Additive (Including Labeling), Submission of Information to a
Master File in Support of Petitions, and Electronic Submission Using FDA Form 3503 ..................................
Radioactive Drug Research Committees ..............................................................................................................
Rapid Response Surveys ......................................................................................................................................
Cosmetic Labeling and Voluntary Cosmetic Registration .....................................................................................
Voluntary National Retail Food Regulatory Program Standards ..........................................................................
FDA’s Voluntary Qualified Importer Program; Guidance for Industry ...................................................................
GFI: E6(R2) Good Clinical Practice; International Council for Harmonisation .....................................................
List of US Manufacturers of Specific CVM-Regulated Products with Interest in Exporting Covered Products to
China ..................................................................................................................................................................
Dated: November 5, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for
Policy.
[FR Doc. 2020–25022 Filed 11–10–20; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission to OMB for
Review and Approval: Public Comment
Request; Information Collection
Request Title: Title V Maternal and
Child Health Services Block Grant to
States Program: Guidance and Forms
for the Title V Application/Annual
Report OMB No. 0915–0172—Revision
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
jbell on DSKJLSW7X2PROD with NOTICES
AGENCY:
In compliance with of the
Paperwork Reduction Act of 1995,
HRSA has submitted an Information
Collection Request (ICR) to the Office of
Management and Budget (OMB) for
review and approval. Comments
submitted during the first public review
SUMMARY:
VerDate Sep<11>2014
17:07 Nov 10, 2020
Jkt 253001
of this ICR will be provided to OMB.
OMB will accept further comments from
the public during the review and
approval period. OMB may act on
HRSA’s ICR only after the 30 day
comment period for this notice has
closed.
DATES: Comments on this ICR must be
received no later than December 14,
2020.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under Review—Open for
Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT: To
request a copy of the clearance requests
submitted to OMB for review, email Lisa
Wright-Solomon, the HRSA Information
Collection Clearance Officer at
paperwork@hrsa.gov or call (301) 443–
1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
information request collection title for
reference.
Information Collection Request Title:
Title V Maternal and Child Health
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
Date approval
expires
0910–0016
0910–0053
0910–0500
0910–0599
0910–0621
0910–0840
0910–0843
09/30/2023
09/30/2023
09/30/2023
09/30/2023
09/30/2023
09/30/2023
09/30/2023
0910–0884
09/30/2023
Services Block Grant to States Program:
Guidance and Forms for the Title V
Application/Annual Report OMB No.
0915–0172—Revision.
Abstract: HRSA is updating the Title
V Maternal and Child Health Services
Block Grant to States Program:
Guidance and Forms for the Title V
Application/Annual Report. This
Guidance is used annually by the 50
states and nine jurisdictions (hereafter
referred to as ‘‘state’’) in applying for
Block Grants under Title V of the Social
Security Act and in preparing the
required Annual Report. The updates
being proposed by HRSA’s Maternal and
Child Health Bureau (MCHB) for this
edition of the Guidance continue to
honor the federal-state partnership that
is supported by the Title V Maternal and
Child Health Services Block Grant and
reinforce the state’s role in developing
a Five-Year Action Plan that addresses
its individual priority needs. These
proposed updates build on and further
refine the reporting structure and vision
that was outlined in the previous
edition. As such, they are intended to
enable a state to provide an articulate
and comprehensive description of its
Title V program activities and its
leadership efforts in advancing and
assuring a public health system that
serves the Maternal and Child Health
population. HRSA’s proposed updates
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12NON1
]]>Agencies
[Federal Register Volume 85, Number 219 (Thursday, November 12, 2020)]
[Notices]
[Page 71925]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-25022]
[[Page 71925]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2020-N-0908; FDA-2010-N-0583; FDA-2020-N-0257; FDA-
2008-N-0490; FDA-2011-N-0017; FDA-2011-N-0144; FDA-2015-D-3327; FDA-
2020-N-1207]
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,
[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
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
----------------------------------------------------------------------------------------------------------------
Submission of Petitions: Food Additive, Color Additive (Including Labeling), 0910-0016 09/30/2023
Submission of Information to a Master File in Support of Petitions, and
Electronic Submission Using FDA Form 3503.....................................
Radioactive Drug Research Committees........................................... 0910-0053 09/30/2023
Rapid Response Surveys......................................................... 0910-0500 09/30/2023
Cosmetic Labeling and Voluntary Cosmetic Registration.......................... 0910-0599 09/30/2023
Voluntary National Retail Food Regulatory Program Standards.................... 0910-0621 09/30/2023
FDA's Voluntary Qualified Importer Program; Guidance for Industry.............. 0910-0840 09/30/2023
GFI: E6(R2) Good Clinical Practice; International Council for Harmonisation.... 0910-0843 09/30/2023
List of US Manufacturers of Specific CVM-Regulated Products with Interest in 0910-0884 09/30/2023
Exporting Covered Products to China...........................................
----------------------------------------------------------------------------------------------------------------
Dated: November 5, 2020.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2020-25022 Filed 11-10-20; 8:45 am]
BILLING CODE 4164-01-P
