Agency Information Collection Activities: Proposed Collection; Comment Request, 32118-32119 [2012-13207]
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32118
Federal Register / Vol. 77, No. 105 / Thursday, May 31, 2012 / Notices
In December 2000, the President
delegated responsibility for funding,
staffing, and operating the Advisory
Board to HHS, which subsequently
delegated this authority to the CDC.
NIOSH implements this responsibility
for CDC. The charter was issued on
August 3, 2001, renewed at appropriate
intervals, and will expire on August 3,
2013.
Purpose: This Advisory Board is
charged with (a) providing advice to the
Secretary, HHS, on the development of
guidelines under Executive Order
13179; (b) providing advice to the
Secretary, HHS, on the scientific
validity and quality of dose
reconstruction efforts performed for this
program; and (c) upon request by the
Secretary, HHS, advise the Secretary on
whether there is a class of employees at
any Department of Energy facility who
were exposed to radiation but for whom
it is not feasible to estimate their
radiation dose, and on whether there is
reasonable likelihood that such
radiation doses may have endangered
the health of members of this class.
Matters To Be Discussed: The agenda
for the Advisory Board meeting
includes: NIOSH Program Update;
Department of Labor Program Update;
Department of Energy Program Update;
NIOSH 10-Year Program Review
Implementation; SEC petitions for:
Winchester Engineering and Analytical
Center (Winchester, MA), Weldon
Spring Plant (Weldon Spring, MO),
Hanford (1972–1983), Los Alamos
National Laboratory, General Steel
Industries (Granite City, IL), Clarksville
Facility (Clarksville, TN), Mound Plant,
Titanium Alloys Manufacturing
(Niagara Falls, NY), and Medina Facility
(San Antonio, TX); Non-qualifying SEC
Petitions and SEC Petitions Status
Update; Linde Ceramics Work Group
Site Profile Review; and Board Work
Sessions.
The agenda is subject to change as
priorities dictate.
In the event an individual cannot
attend, written comments may be
submitted in accordance with the
redaction policy provided below. Any
written comments received will be
provided at the meeting and should be
submitted to the contact person below
well in advance of the meeting.
Policy on Redaction of Board Meeting
Transcripts (Public Comment): (1) If a
person making a comment gives his or
her name, no attempt will be made to
redact that name. (2) NIOSH will take
reasonable steps to ensure that
individuals making public comment are
aware of the fact that their comments
(including their name, if provided) will
appear in a transcript of the meeting
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posted on a public Web site. Such
reasonable steps include: (a) A
statement read at the start of each public
comment period stating that transcripts
will be posted and names of speakers
will not be redacted; (b) A printed copy
of the statement mentioned in (a) above
will be displayed on the table where
individuals sign up to make public
comments; (c) A statement such as
outlined in (a) above will also appear
with the agenda for a Board Meeting
when it is posted on the NIOSH Web
site; (d) A statement such as in (a) above
will appear in the Federal Register
Notice that announces Board and
Subcommittee meetings. (3) If an
individual in making a statement
reveals personal information (e.g.,
medical information) about themselves
that information will not usually be
redacted. The NIOSH FOIA coordinator
will, however, review such revelations
in accordance with the Freedom of
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, Executive Secretary,
NIOSH, CDC, 1600 Clifton Road, M/S E–
20, Atlanta, Georgia 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: May 23, 2012.
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
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10436 and CMS–
855B]
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: Evaluation of
the Multi-Payer Advanced Primary Care
Practice Demonstration; Use: On
September 16, 2009, the Department of
Health and Human Services announced
the establishment of the Multi-Payer
Advanced Primary Care Practice
(MAPCP) Demonstration, under which
Medicare joined Medicaid and private
insurers as a payer participant in statesponsored initiatives to promote the
principles that characterize advanced
primary care, often referred to as the
‘‘patient-centered medical home’’
(PCMH). CMS selected eight states to
participate in this demonstration:
Maine, Vermont, Rhode Island, New
York, Pennsylvania, North Carolina,
Michigan, and Minnesota. These states
vary on a number of important
dimensions, such as features of their
public (Medicaid) and private insurance
markets, delivery system, prior
experience with medical home
initiatives, and nature of their statesponsored multi-payer initiative.
CMS is conducting an evaluation of
the demonstration to assess the effects
of advanced primary care practice when
supported by Medicare, Medicaid, and
AGENCY:
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srobinson on DSK4SPTVN1PROD with NOTICES
Federal Register / Vol. 77, No. 105 / Thursday, May 31, 2012 / Notices
private health plans. As part of this
evaluation, qualitative and quantitative
data will be collected and analyzed to
answer research questions focused on:
(1) State initiative features and
implementation, including various
payment models; (2) practice
characteristics, particularly medical
home transformation; and (3) outcomes,
including access to and coordination of
care, clinical quality of care and patient
safety, beneficiary experience with care,
patterns of utilization, Medicare and
Medicaid expenditures, and budget
neutrality. This information will help
CMS decide whether the MAPCP
Demonstration model should be
expanded under Medicare, and if so,
what modifications and supports would
be needed to implement similar
innovations in other states and practices
in the future. Form Number: CMS–
10436 (OCN: 0938–New); Frequency:
Yearly; Affected Public: Individuals and
households; Number of Respondents:
472 ; Total Annual Responses: 472;
Total Annual Hours: 478 (For policy
questions regarding this collection
contact Suzanne Goodwin at 410–786–
0226. For all other issues call 410–786–
1326.)
2. Type of Information Collection
Request: New collection; Title of
Information Collection: Medicare
Enrollment Application for Clinics/
Group Practice and Certain Other
Suppliers; Use: The primary function of
the CMS–855B enrollment application
for Clinics, Group Practices and Certain
Other Suppliers is to gather information
from the organization that tells us what
it is, whether it meets certain
qualifications to be a health care
supplier, where it renders services and
information necessary to establish the
correct claims payment. The goal of
evaluating and revising the CMS–855B
enrollment application is to simplify
and clarify the information collection
without jeopardizing our need to collect
specific information. The majority of the
revisions are very minor in nature such
as spelling and formatting corrections,
removal of duplicate fields and
instruction clarification for the
organization/group. The Sections and
Sub-Sections within the form are also
being re-numbered and re-sequenced to
create a more logical flow of the data
collection. In addition, CMS is adding a
data collection for an address to mail
the periodic request for the revalidation
of enrollment information (only if it
differs from other addresses currently
collected). Other than the revalidation
mailing address described above, new
data being collected in this revision
package is a checkbox indicating
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17:53 May 30, 2012
Jkt 226001
whether or not an organization is
wholly owned or operated by a hospital,
the inclusion of a new supplier type
(Centralized Flu Biller) and information
on, if applicable, where the supplier
stores its patient records electronically.
Form Number: CMS–855B (OCN: 0938–
New); Frequency: Yearly; Affected
Public: Individuals and households;
Number of Respondents: 31,000; Total
Annual Responses: 31,000; Total
Annual Hours: 103,000 (For policy
questions regarding this collection
contact Kim McPhillips at 410–786–
5374. 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 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 July 30, 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,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Numberllll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: May 25, 2012.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–13207 Filed 5–30–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–305]
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: Revision of a currently
approved collection. Title of
Information Collection: External Quality
Review Protocols. Use: The results of
Medicare reviews, Medicare
accreditation services, and Medicaid
external quality reviews will be used by
States in assessing the quality of care
provided to Medicaid beneficiaries by
managed care organizations and to
provide information on the quality of
care provided to the general public
upon request. Protocols 1, 2, 3, 4, 5, 7,
and the External Quality Review
Background have been revised since the
publication of the 60-day Federal
Register notice on February 17, 2012 (77
FR 9661). All of the revised protocols
associated with the 60-day notice and
this 30-day notice are in draft and must
not be used until they are approved by
OMB through the PRA process. Form
Number: CMS–R–305 (OCN 0938–0786).
Frequency of Reporting: Yearly. Affected
Public: State, Local or Tribal
Governments. Number of Respondents:
42. Total Annual Responses: 70. Total
Annual Hours: 415,643. (For policy
questions regarding this collection
contact Gary B. Jackson at 410–786–
AGENCY:
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Agencies
[Federal Register Volume 77, Number 105 (Thursday, May 31, 2012)]
[Notices]
[Pages 32118-32119]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-13207]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10436 and CMS-855B]
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: Evaluation of the Multi-Payer Advanced Primary
Care Practice Demonstration; Use: On September 16, 2009, the Department
of Health and Human Services announced the establishment of the Multi-
Payer Advanced Primary Care Practice (MAPCP) Demonstration, under which
Medicare joined Medicaid and private insurers as a payer participant in
state-sponsored initiatives to promote the principles that characterize
advanced primary care, often referred to as the ``patient-centered
medical home'' (PCMH). CMS selected eight states to participate in this
demonstration: Maine, Vermont, Rhode Island, New York, Pennsylvania,
North Carolina, Michigan, and Minnesota. These states vary on a number
of important dimensions, such as features of their public (Medicaid)
and private insurance markets, delivery system, prior experience with
medical home initiatives, and nature of their state-sponsored multi-
payer initiative.
CMS is conducting an evaluation of the demonstration to assess the
effects of advanced primary care practice when supported by Medicare,
Medicaid, and
[[Page 32119]]
private health plans. As part of this evaluation, qualitative and
quantitative data will be collected and analyzed to answer research
questions focused on: (1) State initiative features and implementation,
including various payment models; (2) practice characteristics,
particularly medical home transformation; and (3) outcomes, including
access to and coordination of care, clinical quality of care and
patient safety, beneficiary experience with care, patterns of
utilization, Medicare and Medicaid expenditures, and budget neutrality.
This information will help CMS decide whether the MAPCP Demonstration
model should be expanded under Medicare, and if so, what modifications
and supports would be needed to implement similar innovations in other
states and practices in the future. Form Number: CMS-10436 (OCN: 0938-
New); Frequency: Yearly; Affected Public: Individuals and households;
Number of Respondents: 472 ; Total Annual Responses: 472; Total Annual
Hours: 478 (For policy questions regarding this collection contact
Suzanne Goodwin at 410-786-0226. For all other issues call 410-786-
1326.)
2. Type of Information Collection Request: New collection; Title of
Information Collection: Medicare Enrollment Application for Clinics/
Group Practice and Certain Other Suppliers; Use: The primary function
of the CMS-855B enrollment application for Clinics, Group Practices and
Certain Other Suppliers is to gather information from the organization
that tells us what it is, whether it meets certain qualifications to be
a health care supplier, where it renders services and information
necessary to establish the correct claims payment. The goal of
evaluating and revising the CMS-855B enrollment application is to
simplify and clarify the information collection without jeopardizing
our need to collect specific information. The majority of the revisions
are very minor in nature such as spelling and formatting corrections,
removal of duplicate fields and instruction clarification for the
organization/group. The Sections and Sub-Sections within the form are
also being re-numbered and re-sequenced to create a more logical flow
of the data collection. In addition, CMS is adding a data collection
for an address to mail the periodic request for the revalidation of
enrollment information (only if it differs from other addresses
currently collected). Other than the revalidation mailing address
described above, new data being collected in this revision package is a
checkbox indicating whether or not an organization is wholly owned or
operated by a hospital, the inclusion of a new supplier type
(Centralized Flu Biller) and information on, if applicable, where the
supplier stores its patient records electronically. Form Number: CMS-
855B (OCN: 0938-New); Frequency: Yearly; Affected Public: Individuals
and households; Number of Respondents: 31,000; Total Annual Responses:
31,000; Total Annual Hours: 103,000 (For policy questions regarding
this collection contact Kim McPhillips at 410-786-5374. 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 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 July 30, 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,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number--------, Room C4-26-05, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850.
Dated: May 25, 2012.
Martique Jones,
Director, Regulations Development Group, Division B, Office of
Strategic Operations and Regulatory Affairs.
[FR Doc. 2012-13207 Filed 5-30-12; 8:45 am]
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