Agency Information Collection Activities: Submission for OMB Review; Comment Request, 33301-33302 [2021-13223]
Download as PDF
<![CDATA[
33301
Federal Register / Vol. 86, No. 119 / Thursday, June 24, 2021 / Notices
natural grass field users. The total
burden hours for the research study is
184 hours among all of the 220
respondents. There is no cost to the
respondents other than their time in the
study.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Adult/Adolescent Facility Users ................................
Eligibility Screening Script ....................
Adult and Adolescent Questionnaire ....
Exposure Measurement Form ..............
Eligibility Screening Script ....................
Youth and Child Questionnaire ............
Exposure Measurement Form ..............
Parents/Guardians of Youth/Child Facility Users .....
Youth/Child Facility Users ........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–13435 Filed 6–23–21; 8:45 am]
BILLING CODE 4163–70–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10185]
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:
khammond on DSKJM1Z7X2PROD with NOTICES
Number of
respondents
Type of respondents
VerDate Sep<11>2014
19:19 Jun 23, 2021
Jkt 253001
Comments on the collection(s) of
information must be received by the
OMB desk officer by July 26, 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.
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:
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: Revision of a previously
DATES:
PO 00000
Frm 00096
Fmt 4703
Sfmt 4703
110
100
100
110
100
100
Number of
responses per
respondent
1
1
1
1
1
1
Avg. burden
per response
(in hrs.)
5/60
30/60
20/60
5/60
30/60
20/60
approved collection; Title of
Information Collection: Medicare Part D
Reporting Requirements; Use: Section
1860D–12(b)(3)(D) of the Act provides
broad authority for the Secretary to add
terms to the contracts with Part D
sponsors, including terms that require
the sponsor to provide the Secretary
with information as the Secretary may
find necessary and appropriate.
Pursuant to our statutory authority, we
codified these information collection
requirements for Part D sponsors in
regulation at 42 CFR 423.514(a).
Data collected via the Medicare Part D
reporting requirements will be an
integral resource for oversight,
monitoring, compliance, and auditing
activities necessary to ensure quality
provision of the Medicare Prescription
Drug Benefit to beneficiaries. For all
reporting sections (Enrollment and
Disenrollment, Medication Therapy
Management (MTM) Programs,
Grievances, Improving Drug Utilization
Review Controls, Coverage
Determinations and Redeterminations,
and Employer/Union Sponsored
Sponsors), data are reported
electronically to CMS. The data
collected via the MTM and Grievances
reporting sections are used in the
Medicare Part C and D Star Ratings and
Display Measures. The other reporting
sections’ data are analyzed for program
oversight to ensure the availability,
accessibility, and acceptability of
sponsors’ services, such as coverage
determinations and appeals processes,
and opioid safety edits at the time of
dispensing. Form Number: CMS–10185
(OMB control number: 0938–0992);
Frequency: Yearly; Affected Public:
Business or other for-profits; Number of
Respondents: 814; Total Annual
Responses: 12,575; Total Annual Hours:
16,463. (For policy questions regarding
this collection contact Chanelle Jones at
410–786–8008).
E:\FR\FM\24JNN1.SGM
24JNN1
33302
Federal Register / Vol. 86, No. 119 / Thursday, June 24, 2021 / Notices
Dated: June 17, 2021.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2021–13223 Filed 6–23–21; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Evaluation of LifeSet (New
Collection)
Office of Planning, Research,
and Evaluation; Administration for
Children and Families; HHS.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families (ACF) at the U.S.
Department of Health and Human
Services (HHS) is proposing a new
information collection activity to assess
the impact and implementation of
LifeSet, a program that provides services
and supports to young adults ages 17 to
21 with previous child welfare
involvement. Data collection efforts will
include accessing administrative data
from the child welfare agency, program,
and other private and governmental
databases; surveys of young adults
(participants and those receiving
services as usual); interviews and focus
groups with program and child welfare
agency administrators and staff;
interviews and focus groups with young
adult program participants; and
interviews with other program
stakeholders.
DATES: Comments due within 30 days of
publication. OMB must make a decision
about the collection of information
SUMMARY:
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.
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.
SUPPLEMENTARY INFORMATION:
Description: The proposed
information collection activity is the
first phase of a larger study that intends
to assess the impact and
implementation of LifeSet, a program
that provides services and supports to
young adults ages 17 to 21 with
previous child welfare involvement.
The program aims to support young
adults in their transition from foster care
to independent living in the areas of
education, employment and earnings,
housing and economic well-being,
social support, well-being, health and
safety, and criminal involvement. It
focuses on helping young adults
identify and achieve their goals while
developing the skills necessary for
independent living.
The impact study will assess the
effects of young adults’ participation in
LifeSet on outcomes in the primary (i.e.,
confirmatory) domains of education and
employment, housing stability, social
support, and well-being. These
outcomes have been identified by the
implementing agency as the main areas
they expect to target for positive
program impacts. In addition, the
impact study will explore the effects of
participation in the secondary (i.e.,
exploratory) domains of mental health,
criminal justice system contact, intimate
partner violence, and economic wellbeing. The study will utilize a
randomized controlled design.
Information collection activities will
take place over three years and will
include collection of administrative data
from the state child welfare agency, the
program developer, the local program
provider agencies, the National Student
Clearinghouse, unemployment
insurance and employer wage records,
the National Directory of New Hires, the
state homelessness management
information system, the state
department of corrections, the state
juvenile justice commission, the state
court probation services division, and
the state department of human services
division of family development, as well
as survey interviews with program
participants and young adults receiving
services as usual.
The implementation study will collect
information through phone calls and
site visits to the participating program
and child welfare agency. Information
collection activities include interviews
and focus groups with administrators
and staff from the program developer,
child welfare agency, and program
providers.
This evaluation is part of a larger
project to help ACF build the evidence
base in child welfare through rigorous
evaluation of programs, practices, and
policies. The activities and products
from this project will contribute to
evidence building in child welfare and
help to determine the effectiveness of a
program for youth formerly in foster
care on young adult outcomes.
Respondents: Program participants,
young adults receiving services as usual,
agency and program administrators and
staff, other program stakeholders.
khammond on DSKJM1Z7X2PROD with NOTICES
ANNUAL BURDEN ESTIMATES
Number of
respondents
(total over
request
period)
Instrument
Respondents
Site Visit 1 Interview Guide
for Administrators.
Child Welfare Agency Administrators.
Licensed LifeSet Experts
Provider Agency Administrators
LifeSet Developer Administrators
Child Welfare Agency Administrators.
Site Visit 2 Interview Guide
for Administrators.
VerDate Sep<11>2014
19:19 Jun 23, 2021
Jkt 253001
PO 00000
Frm 00097
Fmt 4703
Number of
responses per
respondent
(total over
request
period)
Average
burden per
response
(in hours)
Total burden
(in hours)
Annual
burden
(in hours)
22
1
1
22
7
22
1
1
22
7
Sfmt 4703
E:\FR\FM\24JNN1.SGM
24JNN1
]]>Agencies
[Federal Register Volume 86, Number 119 (Thursday, June 24, 2021)]
[Notices]
[Pages 33301-33302]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-13223]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10185]
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 July 26, 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.
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: 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: Revision of a previously
approved collection; Title of Information Collection: Medicare Part D
Reporting Requirements; Use: Section 1860D-12(b)(3)(D) of the Act
provides broad authority for the Secretary to add terms to the
contracts with Part D sponsors, including terms that require the
sponsor to provide the Secretary with information as the Secretary may
find necessary and appropriate. Pursuant to our statutory authority, we
codified these information collection requirements for Part D sponsors
in regulation at 42 CFR 423.514(a).
Data collected via the Medicare Part D reporting requirements will
be an integral resource for oversight, monitoring, compliance, and
auditing activities necessary to ensure quality provision of the
Medicare Prescription Drug Benefit to beneficiaries. For all reporting
sections (Enrollment and Disenrollment, Medication Therapy Management
(MTM) Programs, Grievances, Improving Drug Utilization Review Controls,
Coverage Determinations and Redeterminations, and Employer/Union
Sponsored Sponsors), data are reported electronically to CMS. The data
collected via the MTM and Grievances reporting sections are used in the
Medicare Part C and D Star Ratings and Display Measures. The other
reporting sections' data are analyzed for program oversight to ensure
the availability, accessibility, and acceptability of sponsors'
services, such as coverage determinations and appeals processes, and
opioid safety edits at the time of dispensing. Form Number: CMS-10185
(OMB control number: 0938-0992); Frequency: Yearly; Affected Public:
Business or other for-profits; Number of Respondents: 814; Total Annual
Responses: 12,575; Total Annual Hours: 16,463. (For policy questions
regarding this collection contact Chanelle Jones at 410-786-8008).
[[Page 33302]]
Dated: June 17, 2021.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2021-13223 Filed 6-23-21; 8:45 am]
BILLING CODE 4120-01-P
