Agency Information Collection Activities: Submission for OMB Review; Comment Request, 61767-61768 [2021-24396]
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Federal Register / Vol. 86, No. 213 / Monday, November 8, 2021 / Notices
The meeting will be held on
October 20–21, 2021, from 10:00 a.m. to
5:00 p.m., EDT (times subject to
change). The docket is currently open to
receive written comments. Written
comments must be received on or before
October 21, 2021.
SUPPLEMENTARY INFORMATION: Notice is
hereby given of a change in the meeting
of the Advisory Committee on
Immunization Practices (ACIP); October
20, 2021, 10:00 a.m.–5:00 p.m., EDT,
and October 21, 2021, 10:00 a.m.–5:00
p.m., EDT (times subject to change), in
the original FRN.
The virtual meeting was published in
the Federal Register on Wednesday,
September 22, 2021, Volume 86,
Number 181, pages 52683–52684.
The virtual meeting is being amended
to change the date the docket was
opened to receive written public
comments, and updates to the Matters
To Be Considered and Written Public
Comment sections of the notice and
should read as follows:
DATES: The meeting will be held on
October 20–21, 2021, from 10:00 a.m. to
5:00 p.m., EDT (times subject to
change). The public may submit written
comments from October 7, 2021 through
October 21, 2021.
Matters To Be Considered: The agenda
will include discussions on herpes
zoster vaccines, influenza vaccines,
pneumococcal vaccine, and COVID–19
vaccines. Recommendation votes on
herpes zoster vaccine, pneumococcal
vaccine, and COVID–19 vaccines are
scheduled. No Vaccines for Children
(VFC) votes are scheduled. Agenda
items are subject to change as priorities
dictate. For more information on ACIP
please visit the ACIP website: https://
www.cdc.gov/vaccines/acip/.
Written Public Comment: The docket
will be opened to receive written
comments on October 7, 2021. Written
comments must be received on or before
October 21, 2021.
The virtual meeting is open to the
public.
FOR FURTHER INFORMATION CONTACT:
Stephanie Thomas, ACIP Committee
Management Specialist, Centers for
Disease Control and Prevention,
National Center for Immunization and
Respiratory Diseases, 1600 Clifton Road
NE, MS–H24–8, Atlanta, GA 30329–
4027; Telephone: 404–639–8367; Email:
ACIP@cdc.gov.
The Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
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DATES:
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committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
61767
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2021–24322 Filed 11–5–21; 8:45 am]
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[FR Doc. 2021–24320 Filed 11–5–21; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Notice of Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended, and the Determination of
the Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, CDC, pursuant to
Public Law 92–463. The grant
applications and the discussions could
disclose confidential trade secrets or
commercial property such as patentable
material, and personal information
concerning individuals associated with
the grant applications, the disclosure of
which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: Disease, Disability,
and Injury Prevention and Control Special
Emphasis Panel (SEP)—RFA–CK–22–003,
Emerging Infections Sentinel Networks
(EISN) Research.
Date: January 11, 2022.
Time: 10:00 a.m.–5:00 p.m., EST.
Place: Teleconference, Centers for Disease
Control and Prevention, Room 1080, 8
Corporate Square Boulevard, Atlanta, Georgia
30329–4027.
Agenda: To review and evaluate grant
applications.
For Further Information Contact: Gregory
Anderson, M.S., M.P.H., Scientific Review
Officer, National Center for HIV/AIDS, Viral
Hepatitis, STD, and TB Prevention, CDC,
1600 Clifton Road NE, Mailstop US8–1,
Atlanta, Georgia 30329–4027, Telephone:
(404) 718–8833, Email: GAnderson@cdc.gov.
The Director, Strategic Business Initiatives
Unit, Office of the Chief Operating Officer,
Centers for Disease Control and Prevention,
has been delegated the authority to sign
Federal Register notices pertaining to
announcements of meetings and other
committee management activities, for both
the Centers for Disease Control and
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Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10280]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. 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 or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected, and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
SUMMARY:
Comments on the collection(s) of
information must be received by the
OMB desk officer by December 8, 2021.
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 30-day Review—Open
for Public Comments’’ or by using the
search function.
DATES:
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61768
Federal Register / Vol. 86, No. 213 / Monday, November 8, 2021 / Notices
lotter on DSK11XQN23PROD with NOTICES1
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ website address at
website address at: https://
www.cms.gov/Regulations-andGuidance/Legislation/Paperwork
ReductionActof1995/PRA-Listing.html.
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of the
Information Collection: Home Health
Change of Care Notice; Use: The
purpose of the Home Health Change of
Care Notice (HHCCN) is to notify
original Medicare beneficiaries
receiving home health care benefits of
plan of care changes. Home health
agencies (HHAs) are required to provide
written notice to Original Medicare
beneficiaries under various
circumstances involving the reduction
or termination of items and/or services
consistent with Home Health Agencies
Conditions of Participation (COPs).
The home health COP requirements
are set forth in § 1891 [42 U.S.C.
1395bbb] of the Social Security Act (the
Act). The implementing regulations
under 42 CFR 484.10(c) specify that
Medicare patients receiving HHA
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18:37 Nov 05, 2021
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services have rights. The patient has the
right to be informed, in advance about
the care to be furnished, and of any
changes in the care to be furnished. The
HHA must advise the patient in advance
of the disciplines that will furnish care,
and the frequency of visits proposed to
be furnished. The HHA must advise the
patient in advance of any change in the
plan of care before the change is made.’’
Notification is required for covered
and non-covered services listed in the
plan of care (POC). The beneficiary will
use the information provided to decide
whether or not to pursue alternative
options to continue receiving the care
noted on the HHCCN. Form Number:
CMS–10280 (OMB control number:
0938–1196); Frequency: Yearly; Affected
Public: Private Sector (Business or other
for-profits, Not-for-Profit Institutions);
Number of Respondents: 11,157; Total
Annual Responses: 12,385,108; Total
Annual Hours: 824,848. (For policy
questions regarding this collection
contact Jennifer McCormick at 410–786–
2852.)
Dated: November 3, 2021.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2021–24396 Filed 11–5–21; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Notification of Obligation
Target Status for CCDF American
Rescue Plan (ARP) Act Stabilization
Funds (0970–0510)
Office of Child Care (OCC),
Administration for Children and
Families, HHS.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families (ACF), Office of
Child Care (OCC) plans to submit a
generic information collection (GenIC)
request under the umbrella generic:
Generic Clearance for Financial Reports
used for ACF Mandatory Grant
Programs (0970–0510). This request
includes an information collection for
SUMMARY:
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Child Care and Development Fund
(CCDF) state and territory grant
recipients to report obligation progress
of the American Rescue Plan (ARP) Act
Stabilization funds.
Comments due within 14 days of
publication. In compliance with the
requirements of the Paperwork
Reduction Act of 1995, ACF is soliciting
public comment on the specific aspects
of the information collection described
above and below.
DATES:
Copies of the proposed
collection of information can be
obtained and comments may be
submitted by emailing infocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
ADDRESSES:
SUPPLEMENTARY INFORMATION:
Description: ACF programs require
detailed financial information from their
grantees that allows ACF to monitor
various specialized cost categories
within each program, to closely manage
program activities, and to have
sufficient financial information to
enable periodic thorough and detailed
audits. The Generic Clearance for
Financial Reports used for ACF
Mandatory Grant Programs allows ACF
programs to efficiently develop and
receive approval for financial reports
that are tailored to specific funding
recipients and the associated needs of
the program. For more information
about the umbrella generic, see: https://
www.reginfo.gov/public/do/PRAView
Document?ref_nbr=202108-0970-002.
This specific GenIC is to meet the
one-time statutory financial reporting
requirement established by the ARP Act
(Pub. L. 117–2, Sec. 2202). The ARP Act
allocated $24 billion for CCDF for lead
agencies to award subgrants to child
care providers in order to stabilize the
child care market. The ARP Act requires
lead agencies to notify the Secretary of
HHS if they are unable to obligate at
least 50 percent of the Stabilization
funds that are available for subgrants
within 9 months of enactment.
Generic clearance approval is
requested to allow ACF’s OCC to collect
the necessary information from CCDF
lead agencies by the statutory deadline
of December 11, 2021.
Respondents: State and territory
CCDF administrators.
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Agencies
[Federal Register Volume 86, Number 213 (Monday, November 8, 2021)]
[Notices]
[Pages 61767-61768]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-24396]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10280]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. 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 or reinstatement of an
existing collection of information, and to allow a second opportunity
for public comment on the notice. Interested persons are invited to
send comments regarding the burden estimate or any other aspect of this
collection of information, including the necessity and utility of the
proposed information collection for the proper performance of the
agency's functions, the accuracy of the estimated burden, ways to
enhance the quality, utility, and clarity of the information to be
collected, and the use of automated collection techniques or other
forms of information technology to minimize the information collection
burden.
DATES: Comments on the collection(s) of information must be received by
the OMB desk officer by December 8, 2021.
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 30-day Review--
Open for Public Comments'' or by using the search function.
[[Page 61768]]
To obtain copies of a supporting statement and any related forms
for the proposed collection(s) summarized in this notice, you may make
your request using one of following:
1. Access CMS' website address at website address at: https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786-4669.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. The term ``collection of
information'' is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and
includes agency requests or requirements that members of the public
submit reports, keep records, or provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires
federal agencies to publish a 30-day notice in the Federal Register
concerning each proposed collection of information, including each
proposed extension or reinstatement of an existing collection of
information, before submitting the collection to OMB for approval. To
comply with this requirement, CMS is publishing this notice that
summarizes the following proposed collection(s) of information for
public comment:
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of the Information Collection: Home Health
Change of Care Notice; Use: The purpose of the Home Health Change of
Care Notice (HHCCN) is to notify original Medicare beneficiaries
receiving home health care benefits of plan of care changes. Home
health agencies (HHAs) are required to provide written notice to
Original Medicare beneficiaries under various circumstances involving
the reduction or termination of items and/or services consistent with
Home Health Agencies Conditions of Participation (COPs).
The home health COP requirements are set forth in Sec. 1891 [42
U.S.C. 1395bbb] of the Social Security Act (the Act). The implementing
regulations under 42 CFR 484.10(c) specify that Medicare patients
receiving HHA services have rights. The patient has the right to be
informed, in advance about the care to be furnished, and of any changes
in the care to be furnished. The HHA must advise the patient in advance
of the disciplines that will furnish care, and the frequency of visits
proposed to be furnished. The HHA must advise the patient in advance of
any change in the plan of care before the change is made.''
Notification is required for covered and non-covered services
listed in the plan of care (POC). The beneficiary will use the
information provided to decide whether or not to pursue alternative
options to continue receiving the care noted on the HHCCN. Form Number:
CMS-10280 (OMB control number: 0938-1196); Frequency: Yearly; Affected
Public: Private Sector (Business or other for-profits, Not-for-Profit
Institutions); Number of Respondents: 11,157; Total Annual Responses:
12,385,108; Total Annual Hours: 824,848. (For policy questions
regarding this collection contact Jennifer McCormick at 410-786-2852.)
Dated: November 3, 2021.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2021-24396 Filed 11-5-21; 8:45 am]
BILLING CODE 4120-01-P