Agency Information Collection Activities: Proposed Collection; Comment Request, 24033-24034 [2011-10370]
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srobinson on DSKHWCL6B1PROD with NOTICES
Federal Register / Vol. 76, No. 83 / Friday, April 29, 2011 / Notices
492–4452. For all other issues call 410–
786–1326.)
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Territory
Cooperative Agreement for the
Affordable Care Act’s Exchanges; Use:
On March 23, 2010, the President signed
into law the Patient Protection and
Affordable Care Act. On March 30,
2010, the Health Care and Education
Reconciliation Act of 2010 was signed
into law. The two laws are collectively
referred to as the Affordable Care Act.
The Affordable Care Act includes a
wide variety of provisions designed to
expand coverage, provide more health
care choices, enhance the quality of
health care for all Americans, hold
insurance companies more accountable,
and lower health care costs.
The Affordable Care Act provides
each State with the option to set up a
State-operated Health Benefits
Exchange. An Exchange is an organized
marketplace to help consumers and
small businesses buy health insurance
in a way that permits easy comparison
of available plan options based on price,
benefits, and quality. By pooling people
together, reducing transaction costs, and
increasing price and quality
transparency, Exchanges create more
efficient and competitive health
insurance markets for individuals and
small employers. The Exchange will
carry out a number of functions as
required by the Affordable Care Act,
including certifying qualified health
plans, administering premium tax
credits and cost-sharing reductions,
responding to consumer requests for
assistance, and providing an easy-to-use
website and written materials that
individuals can use to assess eligibility
and enroll in health insurance coverage,
and coordinating eligibility for and
enrollment in other state health subsidy
programs, including Medicaid and
CHIP.
Section 1311 of the Affordable Care
Act provides for grants to States for the
planning and establishment of
American Health Benefit Exchanges.
The Secretary is planning to disburse
funds in at least three phases: First, for
planning; second, for early information
technology development; and third, for
implementation. $5 million was made
available for Territories Exchange early
implementation. Five Territories were
eligible to receive a Notice of Grant
Award; four applied and have been
awarded funds. The Commonwealth of
the Northern Mariana Islands did not
apply for this funding opportunity
announcement. States and Territories
are eligible for up to $1 million each
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17:39 Apr 28, 2011
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from this grant announcement, which
will extend for up to twelve months.
Form Number: CMS–10370 (OCN:
0938–1118); Frequency: Occasionally;
Affected Public: State, Local, or Tribal
Governments; Number of Respondents:
4; Number of Responses: 40; Total
Annual Hours: 18,706 hours. (For policy
questions regarding this collection,
contact Katherine Harkins at (301) 492–
4445. For all other issues call (410) 786–
1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web site
at https://www.cms.gov/
PaperworkReductionActof1995/PRAL/
list.asp#TopOfPage or email your
request, including your address, phone
number, OMB number, and CMS
document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office at 410–786–
1326.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
be submitted in one of the following
ways by June 28, 2011:
1. Electronically. You may submit
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) 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.
Dated: April 26, 2011.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2011–10430 Filed 4–28–11; 8:45 am]
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24033
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10388]
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.
1. Type of Information Collection
Request: New collection; Title of
Information Collection: Section 1115
Demonstration HIV and AIDS
Application Template; Use: Section
1115 of the Social Security Act (the Act)
allows the Secretary of the Department
of Health and Human Services (the
Secretary) to waive selected provisions
of section 1902 of the Act for
experimental, pilot, or demonstration
projects (demonstrations), and to
provide Federal Financial Participation
(FFP) for demonstration costs which
would not otherwise be considered as
expenditures under the Medicaid State
plan, when the Secretary finds that the
demonstrations are likely to assist in
promoting the objectives of Medicaid.
While some States have applied for
section 1115 demonstrations, many
have not because the process is long and
often tenuous. The purpose of the
application template is to streamline the
process by collecting the minimally
acceptable amount of information
required to appropriately review a
demonstration request. The template
will minimize the amount of time the
State spends preparing a demonstration
request and it should shorten the review
process because the required
information should be present. Form
AGENCY:
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29APN1
24034
Federal Register / Vol. 76, No. 83 / Friday, April 29, 2011 / Notices
Number: CMS–10388 (OMB#: 0938–
NEW); Frequency: Once; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
56; Total Annual Responses: 6; Total
Annual Hours: 270; (For policy
questions regarding this collection
contact Robin Preston at 410–786–3420.
For all other issues call 410–786–1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web site
at https://www.cms.gov/
PaperworkReductionActof1995/PRAL/
list.asp#TopOfPage or email your
request, including your address, phone
number, OMB number, and CMS
document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office at 410–786–
1326.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
be submitted in one of the following
ways by June 28, 2011:
1. Electronically. You may submit
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) 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.
Dated: April 25, 2011.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2011–10370 Filed 4–28–11; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
srobinson on DSKHWCL6B1PROD with NOTICES
[Document Identifier: CMS–10224]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
AGENCY:
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17:39 Apr 28, 2011
Jkt 223001
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS), Department of Health
and Human Services, 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 function;
(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.
1. Type of Information Collection
Request: Revision of currently approved
collection; Title of Information
Collection: Healthcare Common
Procedure Coding System (HCPCS); Use:
In October 2003, the Secretary of Health
and Human Services delegated the
Center for Medicare and Medicaid
Services (CMS) authority to maintain
and distribute HCPCS Level II Codes. As
a result, the National Panel was
delineated and CMS continued with the
decision-making process under its
current structure, the CMS HCPCS
Workgroup (herein referred to as ‘‘the
Workgroup’’. CMS’ HCPCS Workgroup
is an internal workgroup comprised of
representatives of the major components
of CMS, and private insurers, as well as
other consultants from pertinent Federal
agencies. Currently the application
intake is paper-based. However, the
process has grown and the HCPCS staff
is exploring electronic processes for the
collection and storage of applications.
We have received feedback on the
nature of the application; and have
streamlined the form into a userfriendly application. The content of the
material is the same, but the questions
have been refined in accordance with
comments received from industry
members; and the level of necessity of
the information required to render
quality coding decision as determined
by the CMS workgroup. The information
on the form is used to update the
HCPCS code set. All information is
received and distributed to CMS’
HCPCS workgroup and is reviewed and
discussed at workgroup meetings. In
turn, CMS’ HCPCS workgroup reaches a
decision as to whether a change should
be made to codes in the HCPCS code
set. The respondent who submits the
application form can be anyone who has
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an interest in obtaining a code or
modifying an existing code. However,
respondents are usually manufacturers
of products, or consultants on behalf of
the manufacturer. Form Number: CMS–
10224 (OMB#: 0938–1042); Frequency:
Occasionally; Affected Public: Private
sector, business and other for-profit and
not-for-profit institutions; Number of
Respondents: 300; Total Annual
Responses: 300; Total Annual Hours:
3300. (For policy questions regarding
this collection contact Felicia Eggleston
at 410–786–9287 or Lori Anderson at
410–786–6190. For all other issues call
410–786–1326.)
To be assured consideration,
comments and recommendations for the
proposed information collections must
be received by the OMB desk officer at
the address below, no later than 5 p.m.
on May 31, 2011.
OMB, Office of Information and
Regulatory Affairs, Attention: CMS
Desk Officer, Fax Number: (202) 395–
6974, E-mail:
OIRA_submission@omb.eop.gov.
Dated: April 25, 2011.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2011–10366 Filed 4–28–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–E–0087]
Determination of Regulatory Review
Period for Purposes of Patent
Extension; CONVENIA
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) has determined
the regulatory review period for
CONVENIA and is publishing this
notice of that determination as required
by law. FDA has made the
determination because of the
submission of an application to the
Director of Patents and Trademarks,
Department of Commerce, for the
extension of a patent which claims that
animal drug product.
ADDRESSES: Submit electronic
comments to https://
www.regulations.gov. Submit written
petitions along with three copies and
written comments to the Division of
Dockets Management (HFA–305), Food
SUMMARY:
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Agencies
[Federal Register Volume 76, Number 83 (Friday, April 29, 2011)]
[Notices]
[Pages 24033-24034]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-10370]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10388]
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.
1. Type of Information Collection Request: New collection; Title of
Information Collection: Section 1115 Demonstration HIV and AIDS
Application Template; Use: Section 1115 of the Social Security Act (the
Act) allows the Secretary of the Department of Health and Human
Services (the Secretary) to waive selected provisions of section 1902
of the Act for experimental, pilot, or demonstration projects
(demonstrations), and to provide Federal Financial Participation (FFP)
for demonstration costs which would not otherwise be considered as
expenditures under the Medicaid State plan, when the Secretary finds
that the demonstrations are likely to assist in promoting the
objectives of Medicaid. While some States have applied for section 1115
demonstrations, many have not because the process is long and often
tenuous. The purpose of the application template is to streamline the
process by collecting the minimally acceptable amount of information
required to appropriately review a demonstration request. The template
will minimize the amount of time the State spends preparing a
demonstration request and it should shorten the review process because
the required information should be present. Form
[[Page 24034]]
Number: CMS-10388 (OMB: 0938-NEW); Frequency: Once; Affected
Public: State, Local, or Tribal Governments; Number of Respondents: 56;
Total Annual Responses: 6; Total Annual Hours: 270; (For policy
questions regarding this collection contact Robin Preston at 410-786-
3420. For all other issues call 410-786-1326.)
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS'
Web site at https://www.cms.gov/PaperworkReductionActof1995/PRAL/list.asp#TopOfPage or email your request, including your address, phone
number, OMB number, and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the Reports Clearance Office at 410-786-
1326.
In commenting on the proposed information collections please
reference the document identifier or OMB control number. To be assured
consideration, comments and recommendations must be submitted in one of
the following ways by June 28, 2011:
1. Electronically. You may submit 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) 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.
Dated: April 25, 2011.
Martique Jones,
Director, Regulations Development Group, Division B, Office of
Strategic Operations and Regulatory Affairs.
[FR Doc. 2011-10370 Filed 4-28-11; 8:45 am]
BILLING CODE 4120-01-P