Submission for OMB Review; Generic Program-Specific Performance Progress Report, 5887-5888 [2023-01762]
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Federal Register / Vol. 88, No. 19 / Monday, January 30, 2023 / Notices
When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development.
Attention: Document Identifier/OMB
Control Number: ll, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, please access the CMS PRA
website by copying and pasting the
following web address into your web
browser: https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
lotter on DSK11XQN23PROD with NOTICES1
ADDRESSES:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10110 Manufacturer Submission
of Average Sales Price (ASP) Data for
Medicare Part B Drugs and Biologicals
CMS–10242 Emergency Ambulance
Transports and Beneficiary Signature
Under the 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
requires federal agencies to publish a
60-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
VerDate Sep<11>2014
17:30 Jan 27, 2023
Jkt 259001
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Manufacturer
Submission of Average Sales Price
(ASP) Data for Medicare Part B Drugs
and Biologicals; Use: Section 401 of
Division CC of Title IV of the
Consolidated Appropriations Act
(CAA), 2021 amended section 1847A of
the Social Security Act (the Act) to add
new section 1847A(f)(2) of the Act,
which requires manufacturers without a
Medicaid drug rebate agreement to
report average sales price (ASP)
information to CMS for calendar
quarters beginning on January 1, 2022,
for drugs or biologicals payable under
Medicare Part B and described in
sections 1842(o)(1)(C), (E), or (G) or
1881(b)(14)(B) of the Act, including
items, services, supplies, and products
that are payable under Part B as a drug
or biological. The reported ASP data are
used to establish the Medicare payment
amounts. Form Number: CMS–10110
(OMB control number: 0938–0921);
Frequency: Quarterly; Affected Public:
Private sector, Business or other forprofit; Number of Respondents: 500;
Total Annual Responses: 2,000; Total
Annual Hours: 26,000. (For policy
questions regarding this collection
contact Felicia Brown at 410–786–
9287.)
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: CAHPS Hospice
Survey; Use: CMS is required to collect
and publicly report information on the
quality of services provided by hospices
under provisions in the Social Security
Act. Specifically, sections 1814(i)(5)(A)
through (C) of the Act, as added by
section 3132(a) of the Patient Protection
and Affordable Care Act (PPACA) (Pub.
L. 111–148), required hospices to begin
submitting quality data, based on
measures specified by the Secretary of
the Department of Health and Human
Services (the Secretary) for FY 2014 and
subsequent FYs.
The goal of the survey is to measure
the experiences of patients and their
caregivers with hospice care. The survey
was developed to:
• Provide a source of information
from which selected measures could be
publicly reported to beneficiaries and
their family members as a decision aid
for selection of a hospice program;
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5887
• Aid hospices with their internal
quality improvement efforts and
external benchmarking with other
facilities;
• Provide CMS with information for
monitoring the care provided.
Form Number: CMS–10537 (OMB
control number: 0938–1257); Frequency:
Once; Affected Public: Individuals and
Households; Number of Respondents:
1,140,695; Total Annual Responses:
1,140,695; Total Annual Hours: 198,481.
(For policy questions regarding this
collection contact Lauren Fuentes at
410–786 2290 or 443–618–2123.)
Dated: January 25, 2023.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2023–01822 Filed 1–27–23; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
[0970–0490]
Submission for OMB Review; Generic
Program-Specific Performance
Progress Report
Office of Planning, Research,
and Evaluation, Administration for
Children and Families, HHS.
ACTION: Request for public comments.
AGENCY:
This notice describes the
proposal to extend data collection under
the Administration for Children and
Families (ACF) Generic ProgramSpecific Performance Progress Report
(PPR) (0970–0490). This overarching
generic currently allows ACF program
offices to collect performance and
progress data from recipients and subrecipients who receive funding from
ACF under a discretionary grant or
cooperative agreement. This generic
mechanism provides the opportunity for
ACF program offices to tailor requests
for performance and progress data to
specific funding recipients. ACF is
proposing to include performance and
progress data reporting for mandatory
funding recipients in addition to
discretionary funding recipients. ACF is
also requesting an increase in burden.
DATES: Comments due within 30 days of
publication. OMB must make a decision
about 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
SUMMARY:
E:\FR\FM\30JAN1.SGM
30JAN1
5888
Federal Register / Vol. 88, No. 19 / Monday, January 30, 2023 / Notices
if OMB receives it within 30 days of
publication.
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. You can also obtain
copies of the proposed collection of
information by emailing infocollection@
acf.hhs.gov. Identify all emailed
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: ACF is primarily a grantmaking agency that promotes the
economic and social well-being of
families, children, individuals and
communities with partnerships,
funding, guidance, training and
technical assistance.
Prior to the use of this generic
program-specific PPR, a standard ACF
PPR (#0970–0406) was used for all ACF
discretionary grant and cooperative
agreement awards for post award
reporting. Historically, on the standard
ACF PPR form, ACF required grantees to
only respond to a common set of broad
questions, which often solicited
ADDRESSES:
A generic program-specific PPR that
can be tailored for program-specific
needs allows program offices to collect
useful data in a uniform and systematic
manner. The reporting format allows
program offices to gather uniform
program performance data from each
grantee, allowing aggregation at the
program level to calculate outputs and
outcomes, providing a snapshot and
allowing for longitudinal analysis.
Data from a tailored program-specific
PPR that demonstrates a program’s
successes and challenges have been
useful for accountability purposes, such
as required reports to Congress.
Moreover, it has been useful for program
management and oversight, such as
identifying grantees’ technical
assistance needs and ensuring
compliance with federal and
programmatic regulations and policies.
To review currently approved PPRs
under this generic, see: https://
www.reginfo.gov/public/do/
PRAICList?ref_nbr=202206-0970-004.
Respondents: ACF funding recipients.
Annual Burden Estimates: ACF is
requesting an increase in burden
account for the potential use by nondiscretionary programs and to reflect
use over the past 3 years and anticipated
use in the next 3 years.
Instrument
Total
number of
respondents
Total
number of
responses per
respondent
Average
burden
hours per
response
Total burden
hours
Program Specific PPRs ...................................................................................
900
3
6
16,200
John M. Sweet Jr.,
ACF/OPRE Certifying Officer.
[FR Doc. 2023–01762 Filed 1–27–23; 8:45 am]
BILLING CODE 4184–79–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2023–N–0187]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Premarket
Approval of Medical Devices
AGENCY:
lotter on DSK11XQN23PROD with NOTICES1
qualitative or incomplete information.
This one-size-fits-all approach did not
adequately collect the specific data
needed for particular grant programs or
allow program offices to assess
continuous quality improvement.
Different grant programs vary in
purpose, target population, and
activities. Therefore, a need for program
offices to customize performance
measurements was identified and the
generic program-specific PPR was
developed. Non-discretionary funding
recipients have historically provided
performance and progress data through
program-specific information collection
requests. When subject to the Paperwork
Reduction Act, these collections have
been approved through full information
collection requests.
ACF program offices have provided
feedback that the ability to efficiently
customize performance measurements
would also be helpful for these funding
recipients and therefore, ACF would
like to expand this generic to cover
these non-discretionary funding
recipients as well.
ACF program offices have benefited
from the ability to create and use a
program-specific PPR that is more
effective and includes specific data
elements that reflects a specific
program’s indicators, demographics,
priorities and objectives.
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
announcing an opportunity for public
comment on the proposed collection of
certain information by the Agency.
SUMMARY:
VerDate Sep<11>2014
17:30 Jan 27, 2023
Jkt 259001
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 information
collection associated with premarket
approval of medical devices.
DATES: Submit either electronic or
written comments on the collection of
information by March 31, 2023.
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 March 31,
2023. The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of March 31, 2023. Comments
received by mail/hand delivery/courier
PO 00000
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Fmt 4703
Sfmt 4703
(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
as a manufacturing process. Please note
E:\FR\FM\30JAN1.SGM
30JAN1
]]>Agencies
[Federal Register Volume 88, Number 19 (Monday, January 30, 2023)]
[Notices]
[Pages 5887-5888]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-01762]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
[0970-0490]
Submission for OMB Review; Generic Program-Specific Performance
Progress Report
AGENCY: Office of Planning, Research, and Evaluation, Administration
for Children and Families, HHS.
ACTION: Request for public comments.
-----------------------------------------------------------------------
SUMMARY: This notice describes the proposal to extend data collection
under the Administration for Children and Families (ACF) Generic
Program-Specific Performance Progress Report (PPR) (0970-0490). This
overarching generic currently allows ACF program offices to collect
performance and progress data from recipients and sub-recipients who
receive funding from ACF under a discretionary grant or cooperative
agreement. This generic mechanism provides the opportunity for ACF
program offices to tailor requests for performance and progress data to
specific funding recipients. ACF is proposing to include performance
and progress data reporting for mandatory funding recipients in
addition to discretionary funding recipients. ACF is also requesting an
increase in burden.
DATES: Comments due within 30 days of publication. OMB must make a
decision about 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
[[Page 5888]]
if OMB receives it within 30 days of publication.
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. You can
also obtain copies of the proposed collection of information by
emailing [email protected]. Identify all emailed requests by
the title of the information collection.
SUPPLEMENTARY INFORMATION:
Description: ACF is primarily a grant-making agency that promotes
the economic and social well-being of families, children, individuals
and communities with partnerships, funding, guidance, training and
technical assistance.
Prior to the use of this generic program-specific PPR, a standard
ACF PPR (#0970-0406) was used for all ACF discretionary grant and
cooperative agreement awards for post award reporting. Historically, on
the standard ACF PPR form, ACF required grantees to only respond to a
common set of broad questions, which often solicited qualitative or
incomplete information. This one-size-fits-all approach did not
adequately collect the specific data needed for particular grant
programs or allow program offices to assess continuous quality
improvement. Different grant programs vary in purpose, target
population, and activities. Therefore, a need for program offices to
customize performance measurements was identified and the generic
program-specific PPR was developed. Non-discretionary funding
recipients have historically provided performance and progress data
through program-specific information collection requests. When subject
to the Paperwork Reduction Act, these collections have been approved
through full information collection requests.
ACF program offices have provided feedback that the ability to
efficiently customize performance measurements would also be helpful
for these funding recipients and therefore, ACF would like to expand
this generic to cover these non-discretionary funding recipients as
well.
ACF program offices have benefited from the ability to create and
use a program-specific PPR that is more effective and includes specific
data elements that reflects a specific program's indicators,
demographics, priorities and objectives.
A generic program-specific PPR that can be tailored for program-
specific needs allows program offices to collect useful data in a
uniform and systematic manner. The reporting format allows program
offices to gather uniform program performance data from each grantee,
allowing aggregation at the program level to calculate outputs and
outcomes, providing a snapshot and allowing for longitudinal analysis.
Data from a tailored program-specific PPR that demonstrates a
program's successes and challenges have been useful for accountability
purposes, such as required reports to Congress. Moreover, it has been
useful for program management and oversight, such as identifying
grantees' technical assistance needs and ensuring compliance with
federal and programmatic regulations and policies. To review currently
approved PPRs under this generic, see: https://www.reginfo.gov/public/do/PRAICList?ref_nbr=202206-0970-004.
Respondents: ACF funding recipients.
Annual Burden Estimates: ACF is requesting an increase in burden
account for the potential use by non-discretionary programs and to
reflect use over the past 3 years and anticipated use in the next 3
years.
----------------------------------------------------------------------------------------------------------------
Total number of Average burden
Instrument Total number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Program Specific PPRs....................... 900 3 6 16,200
----------------------------------------------------------------------------------------------------------------
John M. Sweet Jr.,
ACF/OPRE Certifying Officer.
[FR Doc. 2023-01762 Filed 1-27-23; 8:45 am]
BILLING CODE 4184-79-P
