Agency Information Collection Activities: Proposed Collection; Comment Request, 6124-6125 [2012-2774]
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6124
Federal Register / Vol. 77, No. 25 / Tuesday, February 7, 2012 / Notices
or treating practitioner and submitted to
the appropriate DME MAC for an initial
decision. The supplier may also submit
the request on behalf of the physician or
treating practitioner. The physician,
treating practitioner or supplier who
submits the request on behalf of the
physician or treating practitioner, is
referred to as the ‘‘submitter.’’ Under
this demonstration, the submitter will
submit to the DME MAC a request for
prior authorization and all relevant
documentation to support Medicare
coverage of the PMD item.
These demonstrations have been
designed to develop and demonstrate
improved methods for the investigation
and prosecution of fraud in the
provision of care or services under the
health programs established by the
Social Security Act. The information
required under this information
collection request is requested by
Medicare contractors to determine
proper payment or if there is a suspicion
of fraud. For the RAC demonstration,
Medicare contractors may request the
information from providers or suppliers
submitting claims for payment from the
Medicare program when data analysis
indicates aberrant billing patterns or
other information which may present a
vulnerability to the Medicare program.
Under the prior authorization
demonstration, for certain PMDs, with a
history of aberrant billing patterns, this
information is requested in advance to
determine appropriate payment or if
there is a suspicion of fraud. Form
Number: CMS–10421 (OCN 0938–New);
Frequency: Occasionally; Affected
Public: State, Local or Tribal
Governments; Number of Respondents:
479,750; Total Annual Responses:
479,750; Total Annual Hours: 243,060.
(For policy questions regarding this
collection contact Debbie Skinner at
(410) 786–7480. 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 April 9, 2012:
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17:34 Feb 06, 2012
Jkt 226001
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 CMS–10161 (OCN
0938–0979), Room C4–26–05, 7500
Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: February 1, 2012.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–2821 Filed 2–3–12; 11:15 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–668B and CMS–
1557]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services.
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: Extension of a currently
approved collection. Title of
Information Collection: Post Clinical
Laboratory Survey Questionnaire and
Supporting Regulations in 42 CFR
AGENCY:
PO 00000
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Fmt 4703
Sfmt 4703
493.1771, 493.1773, and 493.1777. Use:
Form CMS–668B is used by a Clinical
Laboratory Improvement Amendments
(CLIA) laboratory to express its
satisfaction with the survey process and
to make recommendations for
improvement. Surveyors furnish this
form to all laboratories that receive
either an onsite survey or the Alternate
Quality Assessment Survey (i.e., paper
survey of quality indicators). CMS
Central Office performs an overview
evaluation of the completed forms. Each
calendar year, a summary of the
information collected is sent to the State
and CMS Regional Office. Form
Number: CMS–668B (OCN 0938–0653).
Frequency: Biennially; Affected Public:
Business or other for-profits and not-forprofit institutions. State, Local, or Tribal
Government, Federal Government.
Number of Respondents: 21,000. Total
Annual Responses: 10,500. Total
Annual Hours: 2,625. (For policy
questions regarding this collection
contact Kathleen Todd at (410) 786–
3385. For all other issues call (410) 786–
1326.)
2. Type of Information Collection
Request: Extension of a currently
approved collection. Title of
Information Collection: Survey Report
Form for Clinical Laboratory
Improvement Amendments (CLIA) and
Supporting Regulations in 42 CFR
493.1–493.2001. Use: CMS 1557 is used
to report surveyor findings during a
CLIA survey. For each type of survey
conducted (i.e., initial certification,
recertification, validation, complaint,
addition/deletion of specialty/
subspecialty, transfusion fatality
investigation, or revisit inspections) the
Survey Report Form incorporates the
requirements specified in the CLIA
regulations. Form Number: CMS–1557
(OCN 0938–0544). Frequency:
Biennially. Affected Public: Business or
other for-profit, Not-for-profit
institutions, State, Local or Tribal
Governments and Federal Government.
Number of Respondents: 21,000. Total
Annual Responses: 10,500. Total
Annual Hours: 5,248. (For policy
questions regarding this collection
contact Kathleen Todd at (410) 786–
3385. 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
E:\FR\FM\07FEN1.SGM
07FEN1
Federal Register / Vol. 77, No. 25 / Tuesday, February 7, 2012 / Notices
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 April 9, 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 lllll, Room C4–
26–05, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850.
Dated: January 31, 2012.
Martique Jones,
Director, Regulations Development Group,
Division B Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–2774 Filed 2–6–12; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–29 and CMS–
10366]
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
tkelley on DSK3SPTVN1PROD with NOTICES
AGENCY:
VerDate Mar<15>2010
17:34 Feb 06, 2012
Jkt 226001
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: Request for
Certification as a Rural Health Clinic
Form and Supporting Regulations in 42
CFR 491.1–491.11; Use: The Form
CMS–29, Request for Certification as a
Supplier of Rural Health Clinic (RHC)
Services under the Medicare/Medicaid
Program, is utilized as an application to
be completed by suppliers of RHC
services requesting participation in the
Medicare program. This form initiates
the process of obtaining a decision as to
whether the conditions for certification
are met as a supplier of RHC services.
It also promotes data reduction or
introduction to and retrieval from the
Automated Survey Process Environment
(ASPEN) and related survey and
certification databases by the CMS
Regional Offices. Should any question
arise regarding the structure of the
organization, this information is readily
available. With this renewal request, the
title of the Form CMS–29 is being
revised to better describe the purpose of
the data being collected. Both new and
existing clinics must provide and attest
to the accuracy of specific clinic data as
a part of the RHC certification process.
Therefore, the revised title is ‘‘Form
CMS–29/Verification of Clinic Data—
Rural Health Clinic Program.’’ The Form
CMS–29 is also being revised to remove
Section V, Federal Support. The
information captured under Section V is
not a deciding factor as to whether or
not a clinic meets RHC certification
requirements. Therefore, it is
unnecessary to require facilities to
complete this section as a part of the
certification process; Form Number:
CMS–29 (OCN 0938–0074); Frequency:
Occasionally (initially and then every
six years); Affected Public: Private
Sector (Business or other for-profit and
Not-for-profit institutions); Number of
Respondents: 3,981; Total Annual
Responses: 830; Total Annual Hours:
138. (For policy questions regarding this
´
collection contact Shonte Carter at (410)
786–3532. For all other issues call (410)
786–1326.)
2. 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
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6125
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.
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 March 8, 2012. OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer. Fax
Number: (202) 395–6974. Email:
OIRA_submission@omb.eop.gov.
Dated: January 31, 2012.
Martique Jones,
Director, Regulations Development Group,
Division-B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–2762 Filed 2–6–12; 8:45 am]
BILLING CODE 4120–01–P
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07FEN1
Agencies
[Federal Register Volume 77, Number 25 (Tuesday, February 7, 2012)]
[Notices]
[Pages 6124-6125]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-2774]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-668B and CMS-1557]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services.
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: Extension of a currently
approved collection. Title of Information Collection: Post Clinical
Laboratory Survey Questionnaire and Supporting Regulations in 42 CFR
493.1771, 493.1773, and 493.1777. Use: Form CMS-668B is used by a
Clinical Laboratory Improvement Amendments (CLIA) laboratory to express
its satisfaction with the survey process and to make recommendations
for improvement. Surveyors furnish this form to all laboratories that
receive either an onsite survey or the Alternate Quality Assessment
Survey (i.e., paper survey of quality indicators). CMS Central Office
performs an overview evaluation of the completed forms. Each calendar
year, a summary of the information collected is sent to the State and
CMS Regional Office. Form Number: CMS-668B (OCN 0938-0653). Frequency:
Biennially; Affected Public: Business or other for-profits and not-for-
profit institutions. State, Local, or Tribal Government, Federal
Government. Number of Respondents: 21,000. Total Annual Responses:
10,500. Total Annual Hours: 2,625. (For policy questions regarding this
collection contact Kathleen Todd at (410) 786-3385. For all other
issues call (410) 786-1326.)
2. Type of Information Collection Request: Extension of a currently
approved collection. Title of Information Collection: Survey Report
Form for Clinical Laboratory Improvement Amendments (CLIA) and
Supporting Regulations in 42 CFR 493.1-493.2001. Use: CMS 1557 is used
to report surveyor findings during a CLIA survey. For each type of
survey conducted (i.e., initial certification, recertification,
validation, complaint, addition/deletion of specialty/subspecialty,
transfusion fatality investigation, or revisit inspections) the Survey
Report Form incorporates the requirements specified in the CLIA
regulations. Form Number: CMS-1557 (OCN 0938-0544). Frequency:
Biennially. Affected Public: Business or other for-profit, Not-for-
profit institutions, State, Local or Tribal Governments and Federal
Government. Number of Respondents: 21,000. Total Annual Responses:
10,500. Total Annual Hours: 5,248. (For policy questions regarding this
collection contact Kathleen Todd at (410) 786-3385. 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
[[Page 6125]]
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 April 9, 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: January 31, 2012.
Martique Jones,
Director, Regulations Development Group, Division B Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2012-2774 Filed 2-6-12; 8:45 am]
BILLING CODE 4120-01-P