Agency Information Collection Activities: Submission for OMB Review; Comment Request, 29269-29270 [2016-11080]
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Federal Register / Vol. 81, No. 91 / Wednesday, May 11, 2016 / Notices
CMS–10295 (OMB control number:
0938–1073). Frequency: Quarterly;
Affected Public: State, Local, or Tribal
Governments; Number of Respondents:
50; Total Annual Responses: 200; Total
Annual Hours: 400. (For policy
questions regarding this collection
contact Martin Burian at 410–786–
3246.)
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Cooperative
Agreement to Support Navigators in
Federally-facilitated and State
Partnership Exchanges; Use: Section
1311(i) of the Affordable Care Act
requires Exchanges to establish a
Navigator grant program as part of its
function to provide consumers with
assistance when they need it. Navigators
will assist consumers by providing
education about and facilitating
selection of qualified health plans
(QHPs) within Exchanges, as well as
other required duties. Section 1311(i)
requires that an Exchange operating as
of January 1, 2014, must establish a
Navigator Program under which it
awards grants to eligible individuals or
entities who satisfy the requirements to
be Exchange Navigators. In States with
a Federally-facilitated Marketplace
(FFM) or State Partnership Marketplace
(SPM), CMS will be awarding these
grants. Navigator awardees must
provide weekly, monthly, quarterly, and
annual progress reports to CMS on the
activities performed during the grant
period and any sub-awardees receiving
funds. Form Number: CMS–10463
(OMB control number: 0938–1215);
Frequency: Annually, Quarterly,
Monthly, Weekly; Affected Public:
Private sector; Number of Respondents:
102; Total Annual Responses: 102; Total
Annual Hours: 74,188. (For policy
questions regarding this collection,
contact Gian Johnson at 301–492–4323.)
Dated: May 6, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–11078 Filed 5–10–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–484, CMS–846,
854, 847, 848, 849, 10125, 10126, and CMS–
10152]
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 a 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 by June 10, 2016.
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,
SUMMARY:
PO 00000
Frm 00021
Fmt 4703
Sfmt 4703
29269
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:
Attending Physician’s Certification of
Medical Necessity and Supporting
Documentation Requirements; Use: The
certificates of medical necessity (CMNs)
collect information required to help
determine the medical necessity of
certain items. CMS requires CMNs
where there may be a vulnerability to
the Medicare program. Each initial
claim for these items must have an
associated CMN for the beneficiary.
Suppliers (those who bill for the items)
complete the administrative information
(e.g., patient’s name and address, items
ordered, etc.) on each CMN. The 1994
Amendments to the Social Security Act
require that the supplier also provide a
narrative description of the items
ordered and all related accessories, their
charge for each of these items, and the
Medicare fee schedule allowance (where
applicable). The supplier then sends the
CMN to the treating physician or other
clinicians (e.g., physician assistant,
LPN, etc.) who completes questions
pertaining to the beneficiary’s medical
condition and signs the CMN. The
physician or other clinician returns the
CMN to the supplier who has the option
to maintain a copy and then submits the
CMN (paper or electronic) to CMS,
E:\FR\FM\11MYN1.SGM
11MYN1
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29270
Federal Register / Vol. 81, No. 91 / Wednesday, May 11, 2016 / Notices
along with a claim for reimbursement.
Form Number: CMS–484 (OMB control
number: 0938–0534); Frequency:
Occasionally; Affected Public: Private
Sector (Business or other for-profits,
Not-for-profits); Number of
Respondents: 8,880; Total Annual
Responses: 1,632,000; Total Annual
Hours: 326,500; (For policy questions
regarding this collection contact Paula
Smith at 410–786–4709.)
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Durable Medical
Equipment Medicare Administrative
Contractors (MAC) Regional Carrier,
Certificate of Medical Necessity and
Supporting Documentation; Use: The
certificates of medical necessity (CMNs)
collect information required to help
determine the medical necessity of
certain items. CMS requires CMNs
where there may be a vulnerability to
the Medicare program. Each initial
claim for these items must have an
associated CMN for the beneficiary.
Suppliers (those who bill for the items)
complete the administrative information
(e.g., patient’s name and address, items
ordered, etc.) on each CMN. The 1994
Amendments to the Social Security Act
require that the supplier also provide a
narrative description of the items
ordered and all related accessories, their
charge for each of these items, and the
Medicare fee schedule allowance (where
applicable). The supplier then sends the
CMN to the treating physician or other
clinicians (e.g., physician assistant,
LPN, etc.) who completes questions
pertaining to the beneficiary’s medical
condition and signs the CMN. The
physician or other clinician returns the
CMN to the supplier who has the option
to maintain a copy and then submits the
CMN (paper or electronic) to CMS,
along with a claim for reimbursement.
Form Number: CMS–846–849, 854,
10125 and 10126 (OMB control number:
0938–0679); Frequency: Occasionally;
Affected Public: Private Sector (Business
or other for-profits, Not-for-profits);
Number of Respondents: 462,000; Total
Annual Responses: 462,000; Total
Annual Hours: 418,563; (For policy
questions regarding this collection
contact Paula Smith at 410–786–4709.)
3. Type of Information Collection
Request: Extension of a previously
approved collection; Title: Data
Collection for Medicare Beneficiaries
Receiving NaF–18 Positron Emission
Tomography (PET) to Identify Bone
Metastasis in Cancer; Use: In Decision
Memorandum #CAG–00065R, issued on
February 26, 2010, the Centers for
Medicare and Medicaid Services (CMS)
determined that the evidence is
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17:20 May 10, 2016
Jkt 238001
sufficient to conclude that for Medicare
beneficiaries receiving NaF–18 PET scan
to identify bone metastasis in cancer is
reasonable and necessary only when the
provider is participating in and patients
are enrolled in a clinical study designed
to information at the time of the scan to
assist in initial antitumor treatment
planning or to guide subsequent
treatment strategy by the identification,
location and quantification of bone
metastases in beneficiaries in whom
bone metastases are strongly suspected
based on clinical symptoms or the
results of other diagnostic studies.
Qualifying clinical studies must ensure
that specific hypotheses are addressed;
appropriate data elements are collected;
hospitals and providers are qualified to
provide the PET scan and interpret the
results; participating hospitals and
providers accurately report data on all
Medicare enrolled patients; and all
patient confidentiality, privacy, and
other Federal laws must be followed.
Consistent with section 1142 of the
Social Security Act (the Act), the
Agency for Healthcare Research and
Quality (AHRQ) supports clinical
research studies that CMS determines
meets specified standards and address
the specified research questions. To
qualify for payment, providers must
prescribe certain NaF–18 PET scans for
beneficiaries with a set of clinical
criteria specific to each solid tumor. The
statuary authority for this policy is
section 1862 (a)(1)(E) of the Act. The
need to prospectively collect
information at the time of the scan is to
assist the provider in decision making
for patient management. Form Number:
CMS–10152 (OCN: 0938–0968);
Frequency: Annually; Affected Public:
Private Sector (Business or other forprofits); Number of Respondents:
25,000; Total Annual Responses:
25,000; Total Annual Hours: 2,084
hours. (For policy questions regarding
this collection contact Stuart Caplan at
410–786–8564.)
Dated: May 6, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–11080 Filed 5–10–16; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
New Funding Formula
Administration on
Intellectual and Developmental
AGENCIES:
PO 00000
Frm 00022
Fmt 4703
Sfmt 4703
Disabilities (AIDD), Administration on
Disabilities (AoD), Administration for
Community Living (ACL), Department
of Health and Human Services (HHS).
ACTION: Notice.
The Administration on
Intellectual and Developmental
Disabilities (AIDD) within the
Administration on Disabilities (AoD),
located within the Administration for
Community Living (ACL) at the United
States Department of Health and Human
Services (HHS), has developed a new
funding formula for the State Councils
on Developmental Disabilities (SCDD)
and Protection and Advocacy Systems
(P&A) located in each State and
Territory.
SUMMARY:
Effective Date October 1, 2016.
The new formula is printed
below and the estimated allotments for
FY 2017 for each SCDD and P&A can be
found at: https://www.acl.gov/About_
ACL/Allocations/DD-Act.aspx.
FOR FURTHER INFORMATION CONTACT:
Andrew Morris, Office of the
Commissioner, Administration on
Disabilities, 330 C St. SW., Washington,
DC 20201. Telephone (202) 795–7408.
Email andrew.morris@acl.hhs.gov.
Please note the telephone number is not
toll free. This document will be made
available in alternative formats upon
request. Written correspondence can be
sent to Administration for Community
Living, U.S. Department of Health and
Human Services, 330 C St. SW.,
Washington, DC 20201.
SUPPLEMENTARY INFORMATION:
DATES:
ADDRESSES:
Background
The Developmental Disabilities
Assistance and Bill of Rights Act of
2000 (Pub. L. 106–402) provides, among
other things, formula grants to States for
the purpose of operating State Councils
on Developmental Disabilities and
Protection & Advocacy Systems for
people with developmental disabilities.
The Developmental Disabilities
Assistance and Bill of Rights Act of
2000 (DD Act) provides authority and
flexibility in Section 122 to determine
the formula for distributing the annual
grant awards as long as the three
statutory factors are met. These factors
are:
1. Total population of the State/
Territory
2. Need for services for people with
developmental disabilities in the State/
Territory
3. Financial need of the State/
Territory
Responding to years of requests for a
modernized funding formula and after a
E:\FR\FM\11MYN1.SGM
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Agencies
[Federal Register Volume 81, Number 91 (Wednesday, May 11, 2016)]
[Notices]
[Pages 29269-29270]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-11080]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-484, CMS-846, 854, 847, 848, 849, 10125,
10126, and CMS-10152]
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 a 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 by June 10, 2016.
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: Attending Physician's
Certification of Medical Necessity and Supporting Documentation
Requirements; Use: The certificates of medical necessity (CMNs) collect
information required to help determine the medical necessity of certain
items. CMS requires CMNs where there may be a vulnerability to the
Medicare program. Each initial claim for these items must have an
associated CMN for the beneficiary. Suppliers (those who bill for the
items) complete the administrative information (e.g., patient's name
and address, items ordered, etc.) on each CMN. The 1994 Amendments to
the Social Security Act require that the supplier also provide a
narrative description of the items ordered and all related accessories,
their charge for each of these items, and the Medicare fee schedule
allowance (where applicable). The supplier then sends the CMN to the
treating physician or other clinicians (e.g., physician assistant, LPN,
etc.) who completes questions pertaining to the beneficiary's medical
condition and signs the CMN. The physician or other clinician returns
the CMN to the supplier who has the option to maintain a copy and then
submits the CMN (paper or electronic) to CMS,
[[Page 29270]]
along with a claim for reimbursement. Form Number: CMS-484 (OMB control
number: 0938-0534); Frequency: Occasionally; Affected Public: Private
Sector (Business or other for-profits, Not-for-profits); Number of
Respondents: 8,880; Total Annual Responses: 1,632,000; Total Annual
Hours: 326,500; (For policy questions regarding this collection contact
Paula Smith at 410-786-4709.)
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Durable Medical
Equipment Medicare Administrative Contractors (MAC) Regional Carrier,
Certificate of Medical Necessity and Supporting Documentation; Use: The
certificates of medical necessity (CMNs) collect information required
to help determine the medical necessity of certain items. CMS requires
CMNs where there may be a vulnerability to the Medicare program. Each
initial claim for these items must have an associated CMN for the
beneficiary. Suppliers (those who bill for the items) complete the
administrative information (e.g., patient's name and address, items
ordered, etc.) on each CMN. The 1994 Amendments to the Social Security
Act require that the supplier also provide a narrative description of
the items ordered and all related accessories, their charge for each of
these items, and the Medicare fee schedule allowance (where
applicable). The supplier then sends the CMN to the treating physician
or other clinicians (e.g., physician assistant, LPN, etc.) who
completes questions pertaining to the beneficiary's medical condition
and signs the CMN. The physician or other clinician returns the CMN to
the supplier who has the option to maintain a copy and then submits the
CMN (paper or electronic) to CMS, along with a claim for reimbursement.
Form Number: CMS-846-849, 854, 10125 and 10126 (OMB control number:
0938-0679); Frequency: Occasionally; Affected Public: Private Sector
(Business or other for-profits, Not-for-profits); Number of
Respondents: 462,000; Total Annual Responses: 462,000; Total Annual
Hours: 418,563; (For policy questions regarding this collection contact
Paula Smith at 410-786-4709.)
3. Type of Information Collection Request: Extension of a
previously approved collection; Title: Data Collection for Medicare
Beneficiaries Receiving NaF-18 Positron Emission Tomography (PET) to
Identify Bone Metastasis in Cancer; Use: In Decision Memorandum #CAG-
00065R, issued on February 26, 2010, the Centers for Medicare and
Medicaid Services (CMS) determined that the evidence is sufficient to
conclude that for Medicare beneficiaries receiving NaF-18 PET scan to
identify bone metastasis in cancer is reasonable and necessary only
when the provider is participating in and patients are enrolled in a
clinical study designed to information at the time of the scan to
assist in initial antitumor treatment planning or to guide subsequent
treatment strategy by the identification, location and quantification
of bone metastases in beneficiaries in whom bone metastases are
strongly suspected based on clinical symptoms or the results of other
diagnostic studies. Qualifying clinical studies must ensure that
specific hypotheses are addressed; appropriate data elements are
collected; hospitals and providers are qualified to provide the PET
scan and interpret the results; participating hospitals and providers
accurately report data on all Medicare enrolled patients; and all
patient confidentiality, privacy, and other Federal laws must be
followed. Consistent with section 1142 of the Social Security Act (the
Act), the Agency for Healthcare Research and Quality (AHRQ) supports
clinical research studies that CMS determines meets specified standards
and address the specified research questions. To qualify for payment,
providers must prescribe certain NaF-18 PET scans for beneficiaries
with a set of clinical criteria specific to each solid tumor. The
statuary authority for this policy is section 1862 (a)(1)(E) of the
Act. The need to prospectively collect information at the time of the
scan is to assist the provider in decision making for patient
management. Form Number: CMS-10152 (OCN: 0938-0968); Frequency:
Annually; Affected Public: Private Sector (Business or other for-
profits); Number of Respondents: 25,000; Total Annual Responses:
25,000; Total Annual Hours: 2,084 hours. (For policy questions
regarding this collection contact Stuart Caplan at 410-786-8564.)
Dated: May 6, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2016-11080 Filed 5-10-16; 8:45 am]
BILLING CODE 4120-01-P