Agency Information Collection Activities: Submission for OMB Review; Comment Request, 12180-12181 [2015-05165]
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12180
Federal Register / Vol. 80, No. 44 / Friday, March 6, 2015 / Notices
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
responses per
respondent
Number of
respondents
Form name
Total
responses
In-class evaluations ...........................................................
Mail/Telephone/Online Surveys .........................................
Focus groups .....................................................................
40,000
12,000
250
1
1
1
40,000
12,000
250
Total ............................................................................
52,250
1
52,250
Jackie Painter,
Director, Division of the Executive Secretariat.
[FR Doc. 2015–05187 Filed 3–5–15; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–1557, CMS–
10531 and CMS–10535]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
ACTION:
Notice.
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the 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 on the collection(s) of
information must be received by the
OMB desk officer April 6, 2015.
ADDRESSES: When commenting on the
proposed information collections,
please reference the document identifier
or OMB control number. To be assured
mstockstill on DSK4VPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
18:59 Mar 05, 2015
Jkt 235001
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions: OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer, Fax
Number: (202) 395–5806 or Email:
OIRA_submission@omb.eop.gov.
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 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.
Under the
Paperwork Reduction Act of 1995 (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 (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-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 that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Survey Report
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
Average
burden per
response
(in hours)
.05
.25
1.5
.103
Total burden
hours
2,000
3,000
375
5,375
Form for Clinical Laboratory
Improvement Amendments (CLIA) and
Supporting Regulations; Use: The form
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 (OMB control number:
0938–0544); Frequency: Biennially;
Affected Public: Private sector (Business
or other for-profit and Not-for-profit
institutions, State, Local or Tribal
Governments and Federal Government);
Number of Respondents: 19,051; Total
Annual Responses: 9,526; Total Annual
Hours: 4,763. (For policy questions
regarding this collection contact
Kathleen Todd at 410–786–3385).
2. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Transcatheter
Mitral Valve Repair (TMVR) National
Coverage Decision (NCD); Use: The data
collection is required by the Centers for
Medicare and Medicaid Services (CMS)
National Coverage Determination (NCD)
entitled, ‘‘Transcatheter Mitral Valve
Repair (TMVR)’’. The TMVR device is
only covered when specific conditions
are met including that the heart team
and hospital are submitting data in a
prospective, national, audited registry.
The data includes patient, practitioner
and facility level variables that predict
outcomes such as all-cause mortality
and quality of life.
We find that the Society of Thoracic
Surgery/American College of Cardiology
Transcatheter Valve Therapy (STS/ACC
TVT) Registry, one registry overseen by
the National Cardiovascular Data
Registry, meets the requirements
specified in the NCD on TMVR. The
TVT Registry will support a national
surveillance system to monitor the
safety and efficacy of the TMVR
technologies for the treatment of mitral
regurgitation (MR). The data will also
E:\FR\FM\06MRN1.SGM
06MRN1
mstockstill on DSK4VPTVN1PROD with NOTICES
Federal Register / Vol. 80, No. 44 / Friday, March 6, 2015 / Notices
include the variables on the eight item
Kansas City Cardiomyopathy
Questionnaire (KCCQ–10) to assess
heath status, functioning and quality of
life. In the KCCQ, an overall summary
score can be derived from the physical
function, symptoms (frequency and
severity), social function and quality of
life domains. For each domain, the
validity, reproducibility, responsiveness
and interpretability have been
independently established. Scores are
transformed to a range of 0–100, in
which higher scores reflect better health
status.
The conduct of the STS/ACC TVT
Registry and the KCCQ–10 is pursuant
to section 1142 of the Social Security
Act (the ACT) that describes the
authority of the Agency for Healthcare
Research and Quality (AHRQ). Under
section 1142, research may be
conducted and supported on the
outcomes, effectiveness, and
appropriateness of health care services
and procedures to identify the manner
in which disease, disorders, and other
health conditions can be prevented,
diagnosed, treated, and managed
clinically. Section 1862(a)(1)(E) of the
Act allows Medicare to cover under
coverage with evidence development
(CED) certain items or services for
which the evidence is not adequate to
support coverage under section
1862(a)(1)(A) and where additional data
gathered in the context of a clinical
setting would further clarify the impact
of these items and services on the health
of beneficiaries.
The data collected and analyzed in
the TVT Registry will be used to
determine if TMVR is reasonable and
necessary (e.g., improves health
outcomes) for Medicare beneficiaries
under section 1862(a)(1)(A) of the ACT.
Furthermore, data from the Registry will
assist the medical device industry and
the Food and Drug Administration
(FDA) in surveillance of the quality,
safety and efficacy of new medical
devices to treat mitral regurgitation. For
purposes of the TMVR NCD, the TVT
Registry has contracted with the Data
Analytic Centers to conduct the
analyses. In addition, data will be made
available for research purposes under
the terms of a data use agreement that
only provides de-identified datasets.
Form Number: CMS–10531(OMB
control number: 0938–NEW);
Frequency: Annually; Affected Public:
Private sector (Business or other forprofits); Number of Respondents: 4,000;
Total Annual Responses: 16,000; Total
Annual Hours: 5,600. (For policy
questions regarding this collection
contact Roya Lotfi at 410–786–4072).
VerDate Sep<11>2014
18:59 Mar 05, 2015
Jkt 235001
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Employer
Notification to HHS of its Objection to
Providing Coverage for Contraceptive
Services; Use: The proposed rules titled
‘‘Coverage of Certain Preventive
Services Under the Affordable Care Act’’
(79 FR 51118), if finalized as proposed,
would require each qualifying closelyheld, for-profit entity seeking to be
treated as an eligible organization to
provide notification of its religious
objection to coverage of all or a subset
of contraceptive services. Issuers and
third party administrators providing or
arranging payments for contraceptive
services for participants and
beneficiaries in plans of eligible
organizations would be required to meet
the notice requirements as set forth in
the 2013 final regulations, requiring
them to provide notice of the
availability of separate payments for
contraceptive services to participants
and beneficiaries in the eligible
organizations’ plans (78 FR 39870,
39880 (July 2, 2013)).
The interim final regulations titled
‘‘Coverage of Certain Preventive
Services Under the Affordable Care Act’’
(79 FR 51092) continue to allow eligible
organizations that have religious
objections to providing contraceptive
coverage to notify an issuer or third
party administrator using EBSA Form
700, as set forth in the 2013 final
regulations. In addition, these interim
final regulations permit an alternative
process under which an eligible
organization may notify HHS of its
religious objection to coverage of all or
a subset of contraceptive services.
Form Number: CMS–10535 (OMB
control number: 0938–1248); Frequency:
Once; Affected Public: Private sector
(Business or other for-profits and notfor-profit institutions); Number of
Respondents: 61; Number of Responses:
61; Total Annual Hours: 51. (For policy
questions regarding this collection,
contact Usree Bandyopadhyay at 410–
786–6650.)
Dated: March 2, 2015.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2015–05165 Filed 3–5–15; 8:45 am]
BILLING CODE 4120–01–P
PO 00000
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12181
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10464]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates 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.
SUMMARY:
Comments must be received by
May 5, 2015.
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, Division of
Regulations Development, Attention:
Document Identifier/OMB Control
Number lll, Room C4–26–05, 7500
DATES:
E:\FR\FM\06MRN1.SGM
06MRN1
Agencies
[Federal Register Volume 80, Number 44 (Friday, March 6, 2015)]
[Notices]
[Pages 12180-12181]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-05165]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-1557, CMS-10531 and CMS-10535]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (PRA), federal agencies are required to publish notice in
the Federal Register concerning each proposed collection of
information, including each proposed extension or reinstatement of an
existing collection of information, and to allow a second opportunity
for public comment on the notice. Interested persons are invited to
send comments regarding the 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 on the collection(s) of information must be received by
the OMB desk officer April 6, 2015.
ADDRESSES: When commenting on the proposed information collections,
please reference the document identifier or OMB control number. To be
assured consideration, comments and recommendations must be received by
the OMB desk officer via one of the following transmissions: OMB,
Office of Information and Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number: (202) 395-5806 or Email:
OIRA_submission@omb.eop.gov.
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 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: Under the Paperwork Reduction Act of 1995
(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 (44 U.S.C. 3506(c)(2)(A)) requires
federal agencies to publish a 30-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 that
summarizes the following proposed collection(s) of information for
public comment:
1. 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; Use: The form 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 (OMB control number: 0938-0544); Frequency:
Biennially; Affected Public: Private sector (Business or other for-
profit and Not-for-profit institutions, State, Local or Tribal
Governments and Federal Government); Number of Respondents: 19,051;
Total Annual Responses: 9,526; Total Annual Hours: 4,763. (For policy
questions regarding this collection contact Kathleen Todd at 410-786-
3385).
2. Type of Information Collection Request: New collection (Request
for a new OMB control number); Title of Information Collection:
Transcatheter Mitral Valve Repair (TMVR) National Coverage Decision
(NCD); Use: The data collection is required by the Centers for Medicare
and Medicaid Services (CMS) National Coverage Determination (NCD)
entitled, ``Transcatheter Mitral Valve Repair (TMVR)''. The TMVR device
is only covered when specific conditions are met including that the
heart team and hospital are submitting data in a prospective, national,
audited registry. The data includes patient, practitioner and facility
level variables that predict outcomes such as all-cause mortality and
quality of life.
We find that the Society of Thoracic Surgery/American College of
Cardiology Transcatheter Valve Therapy (STS/ACC TVT) Registry, one
registry overseen by the National Cardiovascular Data Registry, meets
the requirements specified in the NCD on TMVR. The TVT Registry will
support a national surveillance system to monitor the safety and
efficacy of the TMVR technologies for the treatment of mitral
regurgitation (MR). The data will also
[[Page 12181]]
include the variables on the eight item Kansas City Cardiomyopathy
Questionnaire (KCCQ-10) to assess heath status, functioning and quality
of life. In the KCCQ, an overall summary score can be derived from the
physical function, symptoms (frequency and severity), social function
and quality of life domains. For each domain, the validity,
reproducibility, responsiveness and interpretability have been
independently established. Scores are transformed to a range of 0-100,
in which higher scores reflect better health status.
The conduct of the STS/ACC TVT Registry and the KCCQ-10 is pursuant
to section 1142 of the Social Security Act (the ACT) that describes the
authority of the Agency for Healthcare Research and Quality (AHRQ).
Under section 1142, research may be conducted and supported on the
outcomes, effectiveness, and appropriateness of health care services
and procedures to identify the manner in which disease, disorders, and
other health conditions can be prevented, diagnosed, treated, and
managed clinically. Section 1862(a)(1)(E) of the Act allows Medicare to
cover under coverage with evidence development (CED) certain items or
services for which the evidence is not adequate to support coverage
under section 1862(a)(1)(A) and where additional data gathered in the
context of a clinical setting would further clarify the impact of these
items and services on the health of beneficiaries.
The data collected and analyzed in the TVT Registry will be used to
determine if TMVR is reasonable and necessary (e.g., improves health
outcomes) for Medicare beneficiaries under section 1862(a)(1)(A) of the
ACT. Furthermore, data from the Registry will assist the medical device
industry and the Food and Drug Administration (FDA) in surveillance of
the quality, safety and efficacy of new medical devices to treat mitral
regurgitation. For purposes of the TMVR NCD, the TVT Registry has
contracted with the Data Analytic Centers to conduct the analyses. In
addition, data will be made available for research purposes under the
terms of a data use agreement that only provides de-identified
datasets. Form Number: CMS-10531(OMB control number: 0938-NEW);
Frequency: Annually; Affected Public: Private sector (Business or other
for-profits); Number of Respondents: 4,000; Total Annual Responses:
16,000; Total Annual Hours: 5,600. (For policy questions regarding this
collection contact Roya Lotfi at 410-786-4072).
3. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Employer
Notification to HHS of its Objection to Providing Coverage for
Contraceptive Services; Use: The proposed rules titled ``Coverage of
Certain Preventive Services Under the Affordable Care Act'' (79 FR
51118), if finalized as proposed, would require each qualifying
closely-held, for-profit entity seeking to be treated as an eligible
organization to provide notification of its religious objection to
coverage of all or a subset of contraceptive services. Issuers and
third party administrators providing or arranging payments for
contraceptive services for participants and beneficiaries in plans of
eligible organizations would be required to meet the notice
requirements as set forth in the 2013 final regulations, requiring them
to provide notice of the availability of separate payments for
contraceptive services to participants and beneficiaries in the
eligible organizations' plans (78 FR 39870, 39880 (July 2, 2013)).
The interim final regulations titled ``Coverage of Certain
Preventive Services Under the Affordable Care Act'' (79 FR 51092)
continue to allow eligible organizations that have religious objections
to providing contraceptive coverage to notify an issuer or third party
administrator using EBSA Form 700, as set forth in the 2013 final
regulations. In addition, these interim final regulations permit an
alternative process under which an eligible organization may notify HHS
of its religious objection to coverage of all or a subset of
contraceptive services.
Form Number: CMS-10535 (OMB control number: 0938-1248); Frequency:
Once; Affected Public: Private sector (Business or other for-profits
and not-for-profit institutions); Number of Respondents: 61; Number of
Responses: 61; Total Annual Hours: 51. (For policy questions regarding
this collection, contact Usree Bandyopadhyay at 410-786-6650.)
Dated: March 2, 2015.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2015-05165 Filed 3-5-15; 8:45 am]
BILLING CODE 4120-01-P