Agency Information Collection Activities: Proposed Collection; Comment Request, 67406-67407 [2015-27859]
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67406
Federal Register / Vol. 80, No. 211 / Monday, November 2, 2015 / Notices
previous extension to this clearance was
published in the Federal Register at 77
FR 56644, on September 13, 2012.
Number of Respondents: 6,601.
Responses per Respondent: 3.
Total Responses: 19,803.
Average Burden Hours per Response:
1.846.
Total Burden Hours: 36,557.
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary for the proper
performance of functions of the Federal
Acquisition Regulation (FAR), and
whether it will have practical utility;
whether our estimate of the public
burden of this collection of information
is accurate, and based on valid
assumptions and methodology; ways to
enhance the quality, utility, and clarity
of the information to be collected; and
ways in which we can minimize the
burden of the collection of information
on those who are to respond, through
the use of appropriate technological
collection techniques or other forms of
information technology.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the General Services Administration,
Regulatory Secretariat Division (MVCB),
1800 F Street NW., Washington, DC
20405, telephone 202–501–4755.
Please cite OMB Control No. 9000–
0149, Subcontract Consent, in all
correspondence.
Edward Loeb,
Acting Director, Federal Acquisition Policy
Division, Office of Governmentwide
Acquisition Policy, Office of Acquisition
Policy, Office of Governmentwide Policy.
[FR Doc. 2015–27819 Filed 10–30–15; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10333]
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
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
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18:55 Oct 30, 2015
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Paperwork Reduction Act of 1995 (the
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
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
Comments must be received by
January 4, 2016.
ADDRESSES: 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 _________, 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, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
DATES:
SUPPLEMENTARY INFORMATION:
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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–10333 Consumer
Assistance Program Grants
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
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: Extension of a currently
approved collection; Title of
Information Collection: Consumer
Assistance Program Grants; Use: Section
1002 of the Affordable Care Act
provides for the establishment of
consumer assistance (or ombudsman)
programs, starting in FY 2010. Federal
grants will support these programs.
These programs will assist consumers
with filing complaints and appeals,
assist consumers with enrollment into
health coverage, collect data on
consumer inquiries and complaints to
identify problems in the marketplace,
educate consumers on their rights and
responsibilities, and with the
establishment of the new Exchange
marketplaces, resolve problems with
premium credits for Exchange coverage.
Importantly, these programs must
provide detailed reporting on the types
of problems and questions consumers
may experience with health coverage,
and how these problems and questions
are resolved. In order to strengthen
oversight, the law requires programs to
report data to the Secretary of the
Department of Health and Human
Services (HHS) ‘‘As a condition of
receiving a grant under subsection (a),
an office of health insurance consumer
assistance or ombudsman program shall
be required to collect and report data to
E:\FR\FM\02NON1.SGM
02NON1
67407
Federal Register / Vol. 80, No. 211 / Monday, November 2, 2015 / Notices
the Secretary on the types of problems
and inquiries encountered by
consumers’’ (Sec. 2793 (d)). Analysis of
this data reporting will help identify
patterns of practice in the insurance
marketplaces and uncover suspected
patterns of noncompliance. HHS must
share program data reports with the
Departments of Labor and Treasury, and
State regulators. Program data also can
offer CCIIO one indication of the
effectiveness of State enforcement,
affording opportunities to provide
technical assistance and support to State
insurance regulators and, in extreme
cases, inform the need to trigger federal
enforcement. Form Number: CMS–
10333 (OMB Control Number: 0938–
1097); Frequency: Annually, Quarterly;
Affected Public: Private Sector: State,
Local, or Tribal Governments; Number
of Respondents: 51; Total Annual
Responses: 459; Total Annual Hours:
9,588. (For policy questions regarding
this collection contact Lateefa Dawkins
at 301–492–4262.)
Dated: October 28, 2015.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2015–27859 Filed 10–30–15; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: Evaluation of the Child Welfare
Capacity Building Collaborative.
OMB No.: New Collection.
Description: The Evaluation of the
Child Welfare Capacity Building
Collaborative is sponsored by the
Children’s Bureau, Administration for
Children and Families of the U.S.
Department of Health and Human
Services. The Capacity Building
Collaborative includes three centers
(Center for States, Center for Tribes,
Center for Courts) funded by the
Children’s Bureau to provide national
child welfare expertise and evidenceinformed training and technical
assistance services to State, Tribal and
Territorial public child welfare agencies
and Court Improvement Programs
(CIPs). The Centers offer a wide array of
services including, but not limited to:
Web-based content and resources,
product development and
dissemination, self-directed and groupbased training, virtual learning and peer
networking events, and tailored
consultation and coaching. During the
project period the Centers’ services will
be evaluated by both Center-specific
evaluations and a Cross-Center
Evaluation. The Center-specific
evaluations are designed to collect data
on Center-specific processes and
outcomes. The Cross-Center Evaluation
is designed to respond to a set of crosscutting evaluation questions posed by
the Children’s Bureau. The Cross-Center
Evaluation will examine: The extent to
which key partners across and within
the Centers are collaborating; whether
the capacity building service
interventions offered by the Centers are
evaluable; the degree to which Centers
follow common protocols; whether
service interventions are delivered or
performed as designed; how satisfied
recipients are with the services
received; how effective the service
interventions were; which service
approaches were most effective and
under what conditions; and the costs of
services.
The Cross-Center Evaluation is
utilizing a longitudinal mixed methods
approach to evaluate the Centers’
services as they develop and mature
over the course of the study period.
Multiple data collection strategies will
be used to efficiently capture
quantitative and qualitative data to
enable analyses that address each
evaluation question. Proposed CrossCenter Evaluation data sources for this
effort include (1) satisfaction surveys to
assess recipients’ satisfaction with
services, such as the Learning
Experiences Satisfaction Survey; (2) a
leadership interview, administered to
all State child welfare directors, Tribal
child welfare directors, and CIP
coordinators that are receiving services
from the Centers; and (3) a collaboration
survey, an annual Web-based survey
administered to the directors and staff of
the three Centers. Center-specific data
sources for this effort include (1)
assessment tools such as the Tribal
Organizational Assessment Caseworker
Interview; and (2) service-specific
feedback forms, such as the Center for
States Intensive Projects instrument and
the Center for Courts CQI Workshops
instrument.
Respondents: Respondents of data
collection instruments will include (1)
child welfare and judicial professionals
that use the Centers’ Web pages,
products, and online courses, that
participate in virtual or in-person
trainings or peer events, and that receive
brief or intensive tailored services from
the Centers; (2) State child welfare
directors, Tribal child welfare directors,
and CIP coordinators that are receiving
services from the Centers; and (3) the
directors and staff of the three Capacity
Building Centers. The proposed data
collection will span four years.
ANNUAL BURDEN ESTIMATES
Annual
number of
respondents
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Instrument
Webpage & Product Satisfaction Survey ........................................................
Learning Experiences Satisfaction Survey ......................................................
Learning Experience Module Survey ..............................................................
Peer Event Satisfaction Survey .......................................................................
Assessment & Capacity Building Plan Satisfaction Survey ............................
Center for Tribes Contact Form .......................................................................
Center for Tribes Demographic Survey ...........................................................
Tribal Organizational Assessment Caseworker Interview ...............................
Tribal Organizational Assessment Community Provider Interview .................
Tribal Organizational Assessment Community Member/Elder Interview ........
Tribal Organizational Assessment Family Interview ........................................
Center for States Information and Referral .....................................................
Center for States Intensive Projects ................................................................
Center for States Constituency Groups ...........................................................
Center for States Consultant Feedback Form .................................................
Center for States Brief Services ......................................................................
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Number of
responses per
respondent
1,560
500
900
5,502
450
50
20
20
16
12
14
12
330
400
156
125
E:\FR\FM\02NON1.SGM
1
1
1
1
1
1
1
1
1
1
1
1
2
2
1
1
02NON1
Average
burden hours
per response
.08
.33
.08
.08
.066
.05
1.75
1.25
1.25
1.0
1.0
.05
.33
.33
.13
.33
Total annual
burden hours
125
165
72
441
30
3
35
25
20
12
14
1
218
264
21
42
Agencies
[Federal Register Volume 80, Number 211 (Monday, November 2, 2015)]
[Notices]
[Pages 67406-67407]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-27859]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10333]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid 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 (the 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 60 days for public
comment on the proposed action. Interested persons are invited to send
comments regarding our burden estimates or any other aspect of this
collection of information, including any of the following subjects: (1)
The necessity and utility of the proposed information collection for
the proper performance of the agency's functions; (2) the accuracy of
the estimated burden; (3) ways to enhance the quality, utility, and
clarity of the information to be collected; and (4) the use of
automated collection techniques or other forms of information
technology to minimize the information collection burden.
DATES: Comments must be received by January 4, 2016.
ADDRESSES: 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 _________, 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, you may make
your request using one of following:
1. Access CMS' Web site address at https://www.cms.hhs.gov/PaperworkReductionActof1995.
2. Email your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at (410) 786-1326.
FOR FURTHER INFORMATION CONTACT: Reports Clearance Office at (410) 786-
1326.
SUPPLEMENTARY INFORMATION:
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-10333 Consumer Assistance Program Grants
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
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: Extension of a currently
approved collection; Title of Information Collection: Consumer
Assistance Program Grants; Use: Section 1002 of the Affordable Care Act
provides for the establishment of consumer assistance (or ombudsman)
programs, starting in FY 2010. Federal grants will support these
programs. These programs will assist consumers with filing complaints
and appeals, assist consumers with enrollment into health coverage,
collect data on consumer inquiries and complaints to identify problems
in the marketplace, educate consumers on their rights and
responsibilities, and with the establishment of the new Exchange
marketplaces, resolve problems with premium credits for Exchange
coverage. Importantly, these programs must provide detailed reporting
on the types of problems and questions consumers may experience with
health coverage, and how these problems and questions are resolved. In
order to strengthen oversight, the law requires programs to report data
to the Secretary of the Department of Health and Human Services (HHS)
``As a condition of receiving a grant under subsection (a), an office
of health insurance consumer assistance or ombudsman program shall be
required to collect and report data to
[[Page 67407]]
the Secretary on the types of problems and inquiries encountered by
consumers'' (Sec. 2793 (d)). Analysis of this data reporting will help
identify patterns of practice in the insurance marketplaces and uncover
suspected patterns of noncompliance. HHS must share program data
reports with the Departments of Labor and Treasury, and State
regulators. Program data also can offer CCIIO one indication of the
effectiveness of State enforcement, affording opportunities to provide
technical assistance and support to State insurance regulators and, in
extreme cases, inform the need to trigger federal enforcement. Form
Number: CMS-10333 (OMB Control Number: 0938-1097); Frequency: Annually,
Quarterly; Affected Public: Private Sector: State, Local, or Tribal
Governments; Number of Respondents: 51; Total Annual Responses: 459;
Total Annual Hours: 9,588. (For policy questions regarding this
collection contact Lateefa Dawkins at 301-492-4262.)
Dated: October 28, 2015.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2015-27859 Filed 10-30-15; 8:45 am]
BILLING CODE 4120-01-P