Agency Information Collection Activities: Proposed Collection; Comment Request, 25406-25407 [2016-09953]
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25406
Federal Register / Vol. 81, No. 82 / Thursday, April 28, 2016 / Notices
Submit comments on or before:
May 31, 2016.
ADDRESSES: Submit comments regarding
this burden estimate or any other aspect
of this collection of information,
including suggestions for reducing this
burden to: Office of Information and
Regulatory Affairs of OMB, Attention:
Desk Officer for GSA, Room 10236,
NEOB, Washington, DC 20503.
Additionally submit a copy to GSA by
any of the following methods:
• Regulations.gov: https://
www.regulations.gov. Submit comments
via the Federal eRulemaking portal by
searching for ‘‘Information Collection
3090–00xx; Simplifying Federal Award
Reporting’’. Select the link ‘‘Submit a
Comment’’ that corresponds with
‘‘Information Collection 3090–00XX;
Simplifying Federal Award Reporting’’.
Follow the instructions provided at the
‘‘Submit a Comment’’ screen. Please
include your name, company name (if
any), and ‘‘Information Collection 3090–
00xx; Simplifying Federal Award
Reporting’’ on your attached document.
• Mail: General Services
Administration, Regulatory Secretariat
Division (MVCB), 1800 F Street NW.,
Washington, DC 20405. ATTN: Ms.
Flowers/IC 3090–00XX, Simplifying
Federal Award Reporting.
Instructions: Please submit comments
only and cite Information Collection
3090–00XX; Simplifying Federal Award
Reporting, in all correspondence related
to this collection. Comments received
generally will be posted without change
to https://www.regulations.gov, including
any personal and/or business
confidential information provided. To
confirm receipt of your comment(s),
please check www.regulations.gov,
approximately two to three days after
submission to verify posting (except
allow 30 days for posting of comments
submitted by mail).
FOR FURTHER INFORMATION CONTACT: Mr.
Kenneth Goldman, GSA, at telephone
202–779–2265.
SUPPLEMENTARY INFORMATION:
DATES:
mstockstill on DSK3G9T082PROD with NOTICES
A. Purpose
The President’s Management Agenda
includes objectives for creating a
twenty-first century government that
delivers better results to the American
people in a more efficient manner.
Leveraging information technology
capabilities to reduce reporting burden
is key to achieving these goals. Section
5 of the Digital Accountability and
Transparency Act (Pub. L. 113–101)
requires a pilot program to develop
recommendations for standardizing
reporting, eliminating unnecessary
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Jkt 238001
duplication, and reducing compliance
costs for recipients of Federal awards.
The pilot participants are required to
provide requested reports as well as the
cost to collect the data via the pilot. The
proposed pilot program will provide an
alternative submission method for
existing Federal Acquisition Regulation
(FAR) requirements, and assess the pilot
results against the existing FAR-required
method.
B. Discussion and Analysis
Comment: ‘‘The best way to simplify
these numerous, massive, expensive
awards is to shut them all down. They
are all fake and mean nothing so who
will miss them. Certainly we all know
they are fake. They are voted on not
because the awarded has done anything
noteworthy. They are simply awards for
being alive. They all need to be cut. The
budget for giving awards should be zero,
totally zero.’’
Response: Thank you for reviewing
the Federal Register Notice. The
comment addresses awards that are part
of a voting process which appears to be
associated with individual personnel
awards. However, the Federal Register
Notice focuses on streamlining reporting
burden for Federal contract awards. If
the comment is intended to address
Federal contract awards, the commenter
is encouraged to visit the Chief
Acquisition Officers Council (CAOC)
National Dialogue: Improving Federal
Procurement and Grants Processes to
engage in a more robust discussion
(link: https://cxo.dialogue2.cao.gov/ ).
C. Annual Reporting Burden
Respondents: 720.
Responses per Respondent: 3 each
week.
Total Annual Responses: 2160.
Hours per Response: .5.
Total Burden Hours: 56,160.
Public comments are particularly
invited on: Whether this collection of
information 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
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
20405, telephone 202–501–4755. Please
cite OMB Control No. 3090–XXXX,
Simplifying Federal Award Reporting,
in all correspondence.
Dated: April 21, 2016.
David A. Shive,
Chief Information Officer.
[FR Doc. 2016–09912 Filed 4–27–16; 8:45 am]
BILLING CODE 6820–61–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10527]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS) is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
estimate 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.
AGENCY:
Comments must be received by
June 27, 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,
DATES:
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28APN1
Federal Register / Vol. 81, No. 82 / Thursday, April 28, 2016 / Notices
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number llll, 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 the following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/Paperwork
ReductionActof1995.
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).
mstockstill on DSK3G9T082PROD with NOTICES
CMS–10527 Annual Eligibility
Redetermination, Product
Discontinuation and Renewal Notices
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.
1. Type of Information Collection
Request: Revision a currently approved
collection; Title of Information
Collection: Annual Eligibility
Redetermination, Product
Discontinuation and Renewal Notices;
Use: Section 1411(f)(1)(B) of the
Affordable Care Act directs the
Secretary of Health and Human Services
(the Secretary) to establish procedures
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22:09 Apr 27, 2016
Jkt 238001
to redetermine the eligibility of
individuals on a periodic basis in
appropriate circumstances. Section
1321(a) of the Affordable Care Act
provides authority for the Secretary to
establish standards and regulations to
implement the statutory requirements
related to Exchanges, QHPs and other
components of title I of the Affordable
Care Act. Under section 2703 of the PHS
Act, as added by the Affordable Care
Act, and sections 2712 and 2741 of the
PHS Act, enacted by the Health
Insurance Portability and
Accountability Act of 1996, health
insurance issuers in the group and
individual markets must guarantee the
renewability of coverage unless an
exception applies.
The final rule ‘‘Patient Protection and
Affordable Care Act; Annual Eligibility
Redeterminations for Exchange
Participation and Insurance
Affordability Programs; Health
Insurance Issuer Standards Under the
Affordable Care Act, Including
Standards Related to Exchanges’’ (79 FR
52994), provides that an Exchange may
choose to conduct the annual
redetermination process for a plan year
(1) in accordance with the existing
procedures described in 45 CFR
155.335; (2) in accordance with
procedures described in guidance
issued by the Secretary for the coverage
year; or (3) using an alternative
proposed by the Exchange and approved
by the Secretary. The guidance
document ‘‘Guidance on Annual
Redeterminations for Coverage for
2015’’ contains the procedures that the
Secretary has specified, as noted in (2)
above, until the issuance of further
guidance. These procedures will be
adopted by the Federally-facilitated
Exchange. Under this option, the
Exchange will provide three notices.
These notices may be combined.
The final rule also amends the
requirements for product renewal and
re-enrollment (or non-renewal) notices
to be sent by Qualified Health Plan
(QHP) issuers in the Exchanges and
specifies content for these notices. The
guidance document ‘‘Draft Updated
Federal Standard Renewal and Product
Discontinuation Notices’’ provides draft
updated Federal standard notices for
product discontinuation and renewal
that would be sent by issuers of
individual market QHPs and issuers in
the individual market. Issuers in the
small group market may use the draft
Federal standard small group notices
released in the June 26, 2014 bulletin
‘‘Draft Standard Notices When
Discontinuing or Renewing a Product in
the Small Group or Individual Market’’,
or any forms of the notice otherwise
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
25407
permitted by applicable laws and
regulations. States that are enforcing the
Affordable Care Act may develop their
own standard notices, for product
discontinuances, renewals, or both,
provided the State-developed notices
are at least as protective as the Federal
standard notices. Form Number: CMS–
10527 (OMB Control Number: 0938–
1254); Frequency: Annually; Affected
Public: Private Sector, State
Governments; Number of Respondents:
2,945; Number of Responses: 12,224;
Total Annual Hours: 149,186. (For
policy questions regarding this
collection, contact Russell Tipps at 301–
492–4371.)
Dated: April 25, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–09953 Filed 4–27–16; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
[CFDA: 93.592]
Announcing the Intent To Award a
Single-Source Expansion Supplement
Grant to the National Domestic
Violence Hotline
Family and Youth Services
Bureau, ACYF, ACF, HHS.
ACTION: This notice announces the
intent to award a single-source
expansion supplement grant under the
Family Violence Prevention and
Services Act (FVPSA) national domestic
violence hotline grant program to the
National Domestic Violence Hotline
(Hotline) in Austin, TX.
AGENCY:
The Administration for
Children and Families (ACF),
Administration on Children, Youth and
Families (ACYF), Family and Youth
Services Bureau (FYSB), Division of
Family Violence and Prevention
Services (DFVPS) announces its intent
to award a cooperative agreement of up
to $3,750,000 as a single-source
expansion supplement to the National
Domestic Violence Hotline (Hotline) in
Austin, TX.
DATES: The period of support for the
single-source expansion supplement is
September 30, 2016 through September
29, 2017.
FOR FURTHER INFORMATION CONTACT:
Angela Yannelli, Senior Program
Specialist, Family Violence Prevention
SUMMARY:
E:\FR\FM\28APN1.SGM
28APN1
Agencies
[Federal Register Volume 81, Number 82 (Thursday, April 28, 2016)]
[Notices]
[Pages 25406-25407]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-09953]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10527]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid
Services (CMS) is publishing the following summary of proposed
collections for public comment. Interested persons are invited to send
comments regarding this burden estimate 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 June 27, 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,
[[Page 25407]]
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 the 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-10527 Annual Eligibility Redetermination, Product Discontinuation
and Renewal Notices
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.
1. Type of Information Collection Request: Revision a currently
approved collection; Title of Information Collection: Annual
Eligibility Redetermination, Product Discontinuation and Renewal
Notices; Use: Section 1411(f)(1)(B) of the Affordable Care Act directs
the Secretary of Health and Human Services (the Secretary) to establish
procedures to redetermine the eligibility of individuals on a periodic
basis in appropriate circumstances. Section 1321(a) of the Affordable
Care Act provides authority for the Secretary to establish standards
and regulations to implement the statutory requirements related to
Exchanges, QHPs and other components of title I of the Affordable Care
Act. Under section 2703 of the PHS Act, as added by the Affordable Care
Act, and sections 2712 and 2741 of the PHS Act, enacted by the Health
Insurance Portability and Accountability Act of 1996, health insurance
issuers in the group and individual markets must guarantee the
renewability of coverage unless an exception applies.
The final rule ``Patient Protection and Affordable Care Act; Annual
Eligibility Redeterminations for Exchange Participation and Insurance
Affordability Programs; Health Insurance Issuer Standards Under the
Affordable Care Act, Including Standards Related to Exchanges'' (79 FR
52994), provides that an Exchange may choose to conduct the annual
redetermination process for a plan year (1) in accordance with the
existing procedures described in 45 CFR 155.335; (2) in accordance with
procedures described in guidance issued by the Secretary for the
coverage year; or (3) using an alternative proposed by the Exchange and
approved by the Secretary. The guidance document ``Guidance on Annual
Redeterminations for Coverage for 2015'' contains the procedures that
the Secretary has specified, as noted in (2) above, until the issuance
of further guidance. These procedures will be adopted by the Federally-
facilitated Exchange. Under this option, the Exchange will provide
three notices. These notices may be combined.
The final rule also amends the requirements for product renewal and
re-enrollment (or non-renewal) notices to be sent by Qualified Health
Plan (QHP) issuers in the Exchanges and specifies content for these
notices. The guidance document ``Draft Updated Federal Standard Renewal
and Product Discontinuation Notices'' provides draft updated Federal
standard notices for product discontinuation and renewal that would be
sent by issuers of individual market QHPs and issuers in the individual
market. Issuers in the small group market may use the draft Federal
standard small group notices released in the June 26, 2014 bulletin
``Draft Standard Notices When Discontinuing or Renewing a Product in
the Small Group or Individual Market'', or any forms of the notice
otherwise permitted by applicable laws and regulations. States that are
enforcing the Affordable Care Act may develop their own standard
notices, for product discontinuances, renewals, or both, provided the
State-developed notices are at least as protective as the Federal
standard notices. Form Number: CMS-10527 (OMB Control Number: 0938-
1254); Frequency: Annually; Affected Public: Private Sector, State
Governments; Number of Respondents: 2,945; Number of Responses: 12,224;
Total Annual Hours: 149,186. (For policy questions regarding this
collection, contact Russell Tipps at 301-492-4371.)
Dated: April 25, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2016-09953 Filed 4-27-16; 8:45 am]
BILLING CODE 4120-01-P