Agency Information Collection Activities: Proposed Collection; Comment Request, 71568-71569 [2011-29840]
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71568
Federal Register / Vol. 76, No. 223 / Friday, November 18, 2011 / Notices
Information Act and the Federal
Advisory Committee Act and if deemed
appropriate, will redact such
information. (4) All disclosures of
information concerning third parties
will be redacted. (5) If it comes to the
attention of the DFO that an individual
wishes to share information with the
Board but objects to doing so in a public
forum, the DFO will work with that
individual, in accordance with the
Federal Advisory Committee Act, to
find a way that the Board can hear such
comments.
CONTACT PERSON FOR MORE INFORMATION:
Theodore Katz, M.P.A., Executive
Secretary, NIOSH, CDC, 1600 Clifton
Road, MS E–20, Atlanta, GA 30333,
telephone: (513) 533–6800, toll free: 1–
(800) CDC–INFO, email: dcas@cdc.gov.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
Notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention, and the Agency for Toxic
Substances and Disease Registry.
Dated: November 9, 2011.
Elaine L. Baker,
Director, Management Analysis and Services
Office Centers for Disease Control and
Prevention.
Management Analysis and Services
Office, CDC, pursuant to Public Law 92–
463.
Matters To Be Discussed: The meeting
will include the initial review,
discussion, and evaluation of
applications received in response to
‘‘National HIV Behavioral Surveillance
For Young Men Who Have Sex With
Men, FOA PS11–0010201SUPP12.’’
Contact Person for More Information:
Amy Yang, Ph.D., Scientific Review
Officer, CDC, 1600 Clifton Road, NE.,
Mailstop E60, Atlanta, Georgia 30333,
Telephone: (404) 718–8836.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Dated: November 8, 2011.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
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Centers for Medicare & Medicaid
Services
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: CMS–10366]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
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The meeting announced below
concerns National HIV Behavioral
Surveillance For Young Men Who Have
Sex With Men, Funding Opportunity
Announcement (FOA), PS11–
0010201SUPP12, initial review.
In accordance with Section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the aforementioned meeting:
Time and Date
1 p.m.–5 p.m., January 12, 2012
(Closed).
Place: Teleconference.
Status: The meeting will be closed to
the public in accordance with
provisions set forth in Section
552b(c)(4) and (6), Title 5 U.S.C., and
the Determination of the Director,
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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.
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1. Type of Information Collection
Request: New collection (request for
new OMB control number); Title of
Information Collection: Nursing Home
Quality Improvement Questionnaire;
Use: The information obtained via the
Nursing Home Quality Improvement
Questionnaire will be utilized by CMS
staff in the Survey & Certification
Group, Division of Nursing Homes, to
identify areas for quality assurance and
performance improvement (QAPI)
technical assistance (TA) that will be
useful to nursing facilities as they
prepare to meet the new QAPI
regulation that was mandated as part of
the Affordable Care Act. Specifically,
the information collected through the
use of the questionnaire will be used to
establish a baseline of QAPI practices in
nursing homes, gather information on
the challenges and barriers to
implementing effective QAPI programs,
assess the development of QAPI
systems, determine what types of TA to
make available to nursing homes, and
assess the potential impact of TA in
advancing QAPI in nursing homes;
Form Number: CMS–10366 (OCN 0938–
New); Frequency: Once; Affected Public:
Private sector (business or other forprofits and not-for-profit institutions)
and State, Local or Tribal Governments;
Number of Respondents: 4,200; Total
Annual Responses: 4,200; Total Annual
Hours: 1,386. (For policy questions
regarding this collection contact Debra
Lyons at (410) 786–6780. 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
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, 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 on (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 January 17, 2012:
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,
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Federal Register / Vol. 76, No. 223 / Friday, November 18, 2011 / Notices
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number lllll, Room C4–
26–05, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850.
Dated: November 15, 2011.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2011–29840 Filed 11–17–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10373]
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
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: Extension of a currently
approved collection; Title of
Information Collection: Medical Loss
Ratio (MLR) Quarterly Reporting for
Mini-Med Plans and Expatriate Plans;
Use: Under Section 2718 of the
Affordable Care Act and implementing
regulations at 45 CFR part 158 (75 FR
74865, December 1, 2010) as modified
by technical corrections on December
30, 2010 (75 FR 82277), a health
insurance issuer (issuer) offering group
or individual health insurance coverage
must submit a report to the Secretary
concerning the amount the issuer
spends each year on claims, quality
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improvement expenses, non-claims
costs, Federal and State taxes and
licensing or regulatory fees, and the
amount of earned premium. An issuer
must provide an annual rebate to
enrollees if the amount it spends on
certain costs compared to its premium
revenue (excluding Federal and States
taxes and licensing or regulatory fees)
does not meet a certain ratio, referred to
as the medical loss ratio (MLR). An
interim final rule (IFR) implementing
the MLR was published on December 1,
2010 (75 FR 74865) and modified by
technical corrections on December 30,
2010 (75 FR 82277), which added part
158 to Title 45 of the Code of Federal
Regulations. The IFR is effective January
1, 2011. Issuers are required to submit
annual MLR reporting data for each
large group market, small group market,
and individual market within each State
in which the issuer conducts business.
For policies that have a total annual
limit of $250,000 or less (sometimes
referred to as ‘‘mini-med plans’’) and for
group policies that primarily cover
employees working outside the United
States (referred to as ‘‘expatriate plans’’),
the IFR applies a special circumstance
adjustment to the MLR data for the 2011
MLR reporting year. In order to evaluate
the appropriateness of this special
circumstance adjustment for years 2012
and beyond, issuers that provide such
policies are required to submit quarterly
MLR data to the Secretary for the 2011
MLR reporting year. We received two
comment letters in response to the 60day comment period that was associated
with CMS–10373. We have taken into
consideration all of the proposed
suggestions, and as result, have not
made any changes to the quarterly
reporting form or to the estimated
burden that correlates with the form.
Form Number: CMS–10373 (OCN:
0938–1132); Frequency: Quarterly;
Affected Public: Private Sector—
Business or other for-profits and Notfor-profit institutions; Number of
Respondents: 75; Total Annual
Responses: 825; Total Annual Hours:
3,700. (For policy questions regarding
this collection contact Carol Jimenez at
(301) 492–4109. 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
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or
Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
PO 00000
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Reports Clearance Office on (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 December 19, 2011.
OMB, Office of Information and
Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number: (202) 395–6974,
Email: OIRA_submission@omb.eop.gov.
Dated: November 15, 2011.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2011–29838 Filed 11–17–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3253–N]
Medicare Program; Meeting of the
Medicare Evidence Development and
Coverage Advisory Committee—
January 25, 2012
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice of meeting.
AGENCY:
This notice announces that a
public meeting of the Medicare
Evidence Development & Coverage
Advisory Committee (MEDCAC)
(‘‘Committee’’) will be held on
Wednesday, January 25, 2012. The
Committee generally provides advice
and recommendations concerning the
adequacy of scientific evidence needed
to determine whether certain medical
items and services can be covered under
the Medicare statute. This meeting will
focus on the currently available
evidence regarding the management of
carotid atherosclerosis. This meeting is
open to the public in accordance with
the Federal Advisory Committee Act
(5 U.S.C. App. 2, section 10(a)).
DATES: Meeting Date: The public
meeting will be held on Wednesday,
January 25, 2012 from 7:30 a.m. until
4:30 p.m., Eastern Standard Time (EST).
Deadline for Submission of Written
Comments: Written comments must be
received at the address specified in the
ADDRESSES section of this notice by
5 p.m. EST, Monday, December 19,
2011. Once submitted, all comments are
final.
Deadlines for Speaker Registration
and Presentation Materials: The
SUMMARY:
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Agencies
[Federal Register Volume 76, Number 223 (Friday, November 18, 2011)]
[Notices]
[Pages 71568-71569]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-29840]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10366]
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 (request
for new OMB control number); Title of Information Collection: Nursing
Home Quality Improvement Questionnaire; Use: The information obtained
via the Nursing Home Quality Improvement Questionnaire will be utilized
by CMS staff in the Survey & Certification Group, Division of Nursing
Homes, to identify areas for quality assurance and performance
improvement (QAPI) technical assistance (TA) that will be useful to
nursing facilities as they prepare to meet the new QAPI regulation that
was mandated as part of the Affordable Care Act. Specifically, the
information collected through the use of the questionnaire will be used
to establish a baseline of QAPI practices in nursing homes, gather
information on the challenges and barriers to implementing effective
QAPI programs, assess the development of QAPI systems, determine what
types of TA to make available to nursing homes, and assess the
potential impact of TA in advancing QAPI in nursing homes; Form Number:
CMS-10366 (OCN 0938-New); Frequency: Once; Affected Public: Private
sector (business or other for-profits and not-for-profit institutions)
and State, Local or Tribal Governments; Number of Respondents: 4,200;
Total Annual Responses: 4,200; Total Annual Hours: 1,386. (For policy
questions regarding this collection contact Debra Lyons at (410) 786-
6780. 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 address at https://www.cms.hhs.gov/PaperworkReductionActof1995,
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 on (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 January 17, 2012:
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,
[[Page 71569]]
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number ----------, Room C4-26-05, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850.
Dated: November 15, 2011.
Martique Jones,
Director, Regulations Development Group, Division B, Office of
Strategic Operations and Regulatory Affairs.
[FR Doc. 2011-29840 Filed 11-17-11; 8:45 am]
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