Agency Information Collection Activities: Proposed Collection; Comment Request, 68851-68852 [2013-27305]
Download as PDF
Federal Register / Vol. 78, No. 221 / Friday, November 15, 2013 / Notices
The duplicate FRN published on
[11/5/13] at [Vol. 78, No. 214 Page
66363] is withdrawn as of [11/12/13].
FOR FURTHER INFORMATION CONTACT:
(404) 639–7570 or send comments to
CDC LeRoy Richardson, 1600 Clifton
Road, MS D–74, Atlanta, GA 30333 or
send an email to omb@cdc.gov.
SUPPLEMENTARY INFORMATION: N/A.
DATES:
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Science Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2013–27403 Filed 11–14–13; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10508, CMS–
10507 and CMS–855A]
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.
DATES: Comments must be received by
January 14, 2014.
ADDRESSES: When commenting, please
reference the document identifier or
emcdonald on DSK67QTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
16:58 Nov 14, 2013
Jkt 232001
OMB control number (OCN). 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 ____, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
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:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10508 Evaluation of the Rural
Community Hospital Demonstration
(RCHD)
CMS–10507 State-based Marketplace
Annual Report (SMAR)
CMS–855A Medicare Enrollment
Application: Medicare Part A
Institutional Providers
Under the Paperwork Reduction Act
(the 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.
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
68851
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-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.
Information Collections
1. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Evaluation of
the Rural Community Hospital
Demonstration (RCHD); Use: Section
10313 of the Affordable Care Act of
2010 (ACA) extended and expanded the
Rural Community Hospital
Demonstration (RCHD). Originally
authorized under the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA), the
RCHD provides enhanced
reimbursement for inpatient services to
small rural hospitals that do not qualify
as critical access hospitals (CAHs). The
RCHD is intended to increase the
capability of these hospitals to meet the
health care needs of rural beneficiaries
in their service areas. As a
demonstration, the RCHD aims to
provide information that can be used to
assess the feasibility and advisability of
establishing a new category of rural
community hospitals for reimbursement
policy. As of January 2013, 23 hospitals
from 11 states are participating in the
RCHD. This number includes seven
hospitals continuing from the original
demonstration as authorized under the
MMA and 15 new hospitals that joined
under the expansion authorized under
the ACA.
For the original demonstration, the
MMA required a Report to Congress six
months after the end of the
demonstration, a requirement
unchanged by the ACA. An initial
evaluation was conducted between 2007
and 2011 toward preparing for a Report
to Congress and focused on the 17
hospitals that had participated at some
point between October 2004 and March
2011. Findings from this evaluation
were reported to the Centers for
Medicare and Medicaid Services (CMS)
in the Interim Evaluation Report of the
Rural Community Hospital
Demonstration (an unpublished report).
The current five-year evaluation of the
RCHD will extend and build on the
prior evaluation and produce the Report
to Congress required by the MMA. It
will assess the impact of the RCHD in
meeting its goals: To enable hospitals to
E:\FR\FM\15NON1.SGM
15NON1
emcdonald on DSK67QTVN1PROD with NOTICES
68852
Federal Register / Vol. 78, No. 221 / Friday, November 15, 2013 / Notices
achieve community benefits such as
improved services for their communities
(especially Medicare beneficiaries),
meet their individual strategic goals,
and improve the financial solvency and
viability of the participating hospitals.
In addition, the evaluation will
determine if it is feasible and advisable
to create a new payment category of
rural hospitals. To achieve this
objective, the evaluation will examine
how RCHD hospitals responded to
payment options and assess how the
costs to Medicare under RCHD compare
to existing alternative payment options.
The evaluation will also summarize
the characteristics of the markets served
by RCHD hospitals, including
beneficiaries’ proximity to inpatient
providers and competition among
providers in the area. The information
will be used to assess the implications
of expanding the RCHD payment system
to hospitals in various market
environments. In addition, the
evaluation will examine the potential
costs of expanding the RCHD payment
methodology, accounting for alternative
approaches to targeting rural hospitals.
Form Number: CMS–10508 (OCN:
0938–NEW); Frequency: Annually;
Affected Public: State, Local or Tribal
Governments, Private sector—Business
or other for-profit and Not-for-profit
organizations; Number of Respondents:
57; Total Annual Responses: 101; Total
Annual Hours: 245. (For policy
questions regarding this collection
contact Woolton Lee at 410–786–4942.)
2. Title of Information Collection:
State-based Marketplace Annual Report
(SMAR); Type of Information Collection
Request: New collection (Request for a
new OMB control number); Use: The
annual report is the primary vehicle to
insure comprehensive compliance with
all reporting requirements contained in
the Affordable Care Act. It is specifically
called for in section 1313(a)(1) of the
Act which requires an State-based
Marketplace (SBM) to keep an accurate
accounting of all activities, receipts, and
expenditures, and to submit a report
annually to the Secretary concerning
such accounting. We will use the
information collected from states to
assist in determining if a state is
maintaining a compliant operational
Exchange. It will also provide a
mechanism to collect innovative
approaches to meeting challenges
encountered by the SBMs during the
preceding year. Additionally, it will
provide information to us regarding
potential changes in priorities and
approaches for the upcoming year. Form
Number: CMS–10507 (OCN: 0938–
NEW); Frequency: Annually; Affected
Public: State, Local, or Tribal
VerDate Mar<15>2010
16:58 Nov 14, 2013
Jkt 232001
governments; Number of Respondents:
19; Number of Responses: 19; Total
Annual Hours: 1,482. (For policy
questions regarding this collection,
contact Shelley Bain at 301–492–4453.)
3. Title of Information Collection:
Medicare Enrollment Application:
Medicare Part A Institutional Providers;
Type of Information Collection Request:
Revision of a currently approved
collection ; Use: We are revising the
CMS–855 Medicare Enrollment
Applications information collection
request to remove the CMS–855I, CMS–
855B and CMS–855R applications from
its collection. We have found that the
regulations governing the enrollment
requirements for health care facilities
occur at intervals separate from the
other provider and supplier types
reimbursed by Medicare. Consequently,
we may need to revise and submit the
CMS–855A enrollment application for
OMB approval at intervals separate from
the other enrollment applications which
include the CMS–855B, CMS–855I and
CMS–855R enrollment applications.
The ability to revise the CMS–855A
separately from the other CMS–855
enrollment applications will lessen the
burden on us and OMB as well as the
public during the Federal Register
notice period, as only one subset of
provider or suppliers will be effected by
CMS–855A revisions. We intend to
maintain the continuity of the CMS–855
enrollment applications by using the
same formats and lay-out of the current
CMS–855 enrollment applications,
regardless of the separation of the CMS
855A from the collective enrollment
application package.
At this time we are also using this
opportunity to make editorial and
clerical corrections to the CMS–855A to
simplify and clarify the current data
collection and to remove obsolete
requirements and data collection. The
sections and sub-sections within the
form are also being re-numbered and resequenced to create a more logical flow
of the data collection. In addition, we
are 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). More
specific information regarding types of
Home Health Agency sub-units will also
be collected. Other than the information
above, new data being collected in this
revision package is information on, if
applicable, where the supplier stores its
patient records electronically.
Form Number: CMS–855A (OCN:
0938–0685); Frequency: Annually;
Affected Public: State, Local, or Tribal
governments; Number of Respondents:
18,000; Number of Responses: 18,000;
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
Total Annual Hours: 78,000. (For policy
questions regarding this collection,
contact Kim McPhillips at 410–786–
5374.)
Dated: November 8, 2013.
Martique Jones,
Deputy Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2013–27305 Filed 11–14–13; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–D–0715]
Draft Guidance for Industry on
Acrylamide in Foods; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or we) is
announcing the availability of a draft
guidance entitled ‘‘Guidance for
Industry: Acrylamide in Foods.’’ The
draft guidance is intended to provide
information that may help growers,
manufacturers, and food service
operators reduce acrylamide in certain
foods. Acrylamide is a chemical that can
form in some foods during certain types
of high-temperature cooking. The draft
guidance is intended to suggest a range
of possible approaches to acrylamide
reduction and not to identify specific
recommended approaches.
DATES: Although you can comment on
any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that we consider
your comment on the draft guidance
before we begin work on the final
version of the guidance, submit either
electronic or written comments on the
draft guidance by January 14, 2014.
ADDRESSES: Submit written requests for
single copies of the draft guidance to the
Office of Food Safety, Center for Food
Safety and Applied Nutrition (HFS–
300), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park,
MD 20740. Send two self-addressed
adhesive labels to assist that office in
processing your request. See the
SUPPLEMENTARY INFORMATION section for
electronic access to the draft guidance.
Submit electronic comments on the
draft guidance to https://
www.regulations.gov. Submit written
comments on the draft guidance to the
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, Rm. 1061, Rockville,
MD 20852.
SUMMARY:
E:\FR\FM\15NON1.SGM
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Agencies
[Federal Register Volume 78, Number 221 (Friday, November 15, 2013)]
[Notices]
[Pages 68851-68852]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-27305]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-10508, CMS-10507 and CMS-855A]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
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 (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.
DATES: Comments must be received by January 14, 2014.
ADDRESSES: When commenting, please reference the document identifier or
OMB control number (OCN). 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 --------, Room C4-26-05, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850.
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:
Contents
This notice sets out a summary of the use and burden associated
with the following information collections. More detailed information
can be found in each collection's supporting statement and associated
materials (see ADDRESSES).
CMS-10508 Evaluation of the Rural Community Hospital Demonstration
(RCHD)
CMS-10507 State-based Marketplace Annual Report (SMAR)
CMS-855A Medicare Enrollment Application: Medicare Part A
Institutional Providers
Under the Paperwork Reduction Act (the 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 requires federal agencies to publish a 60-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.
Information Collections
1. Type of Information Collection Request: New collection (Request
for a new OMB control number); Title of Information Collection:
Evaluation of the Rural Community Hospital Demonstration (RCHD); Use:
Section 10313 of the Affordable Care Act of 2010 (ACA) extended and
expanded the Rural Community Hospital Demonstration (RCHD). Originally
authorized under the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA), the RCHD provides enhanced
reimbursement for inpatient services to small rural hospitals that do
not qualify as critical access hospitals (CAHs). The RCHD is intended
to increase the capability of these hospitals to meet the health care
needs of rural beneficiaries in their service areas. As a
demonstration, the RCHD aims to provide information that can be used to
assess the feasibility and advisability of establishing a new category
of rural community hospitals for reimbursement policy. As of January
2013, 23 hospitals from 11 states are participating in the RCHD. This
number includes seven hospitals continuing from the original
demonstration as authorized under the MMA and 15 new hospitals that
joined under the expansion authorized under the ACA.
For the original demonstration, the MMA required a Report to
Congress six months after the end of the demonstration, a requirement
unchanged by the ACA. An initial evaluation was conducted between 2007
and 2011 toward preparing for a Report to Congress and focused on the
17 hospitals that had participated at some point between October 2004
and March 2011. Findings from this evaluation were reported to the
Centers for Medicare and Medicaid Services (CMS) in the Interim
Evaluation Report of the Rural Community Hospital Demonstration (an
unpublished report).
The current five-year evaluation of the RCHD will extend and build
on the prior evaluation and produce the Report to Congress required by
the MMA. It will assess the impact of the RCHD in meeting its goals: To
enable hospitals to
[[Page 68852]]
achieve community benefits such as improved services for their
communities (especially Medicare beneficiaries), meet their individual
strategic goals, and improve the financial solvency and viability of
the participating hospitals. In addition, the evaluation will determine
if it is feasible and advisable to create a new payment category of
rural hospitals. To achieve this objective, the evaluation will examine
how RCHD hospitals responded to payment options and assess how the
costs to Medicare under RCHD compare to existing alternative payment
options.
The evaluation will also summarize the characteristics of the
markets served by RCHD hospitals, including beneficiaries' proximity to
inpatient providers and competition among providers in the area. The
information will be used to assess the implications of expanding the
RCHD payment system to hospitals in various market environments. In
addition, the evaluation will examine the potential costs of expanding
the RCHD payment methodology, accounting for alternative approaches to
targeting rural hospitals. Form Number: CMS-10508 (OCN: 0938-NEW);
Frequency: Annually; Affected Public: State, Local or Tribal
Governments, Private sector--Business or other for-profit and Not-for-
profit organizations; Number of Respondents: 57; Total Annual
Responses: 101; Total Annual Hours: 245. (For policy questions
regarding this collection contact Woolton Lee at 410-786-4942.)
2. Title of Information Collection: State-based Marketplace Annual
Report (SMAR); Type of Information Collection Request: New collection
(Request for a new OMB control number); Use: The annual report is the
primary vehicle to insure comprehensive compliance with all reporting
requirements contained in the Affordable Care Act. It is specifically
called for in section 1313(a)(1) of the Act which requires an State-
based Marketplace (SBM) to keep an accurate accounting of all
activities, receipts, and expenditures, and to submit a report annually
to the Secretary concerning such accounting. We will use the
information collected from states to assist in determining if a state
is maintaining a compliant operational Exchange. It will also provide a
mechanism to collect innovative approaches to meeting challenges
encountered by the SBMs during the preceding year. Additionally, it
will provide information to us regarding potential changes in
priorities and approaches for the upcoming year. Form Number: CMS-10507
(OCN: 0938-NEW); Frequency: Annually; Affected Public: State, Local, or
Tribal governments; Number of Respondents: 19; Number of Responses: 19;
Total Annual Hours: 1,482. (For policy questions regarding this
collection, contact Shelley Bain at 301-492-4453.)
3. Title of Information Collection: Medicare Enrollment
Application: Medicare Part A Institutional Providers; Type of
Information Collection Request: Revision of a currently approved
collection ; Use: We are revising the CMS-855 Medicare Enrollment
Applications information collection request to remove the CMS-855I,
CMS-855B and CMS-855R applications from its collection. We have found
that the regulations governing the enrollment requirements for health
care facilities occur at intervals separate from the other provider and
supplier types reimbursed by Medicare. Consequently, we may need to
revise and submit the CMS-855A enrollment application for OMB approval
at intervals separate from the other enrollment applications which
include the CMS-855B, CMS-855I and CMS-855R enrollment applications.
The ability to revise the CMS-855A separately from the other CMS-855
enrollment applications will lessen the burden on us and OMB as well as
the public during the Federal Register notice period, as only one
subset of provider or suppliers will be effected by CMS-855A revisions.
We intend to maintain the continuity of the CMS-855 enrollment
applications by using the same formats and lay-out of the current CMS-
855 enrollment applications, regardless of the separation of the CMS
855A from the collective enrollment application package.
At this time we are also using this opportunity to make editorial
and clerical corrections to the CMS-855A to simplify and clarify the
current data collection and to remove obsolete requirements and data
collection. 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, we are 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). More specific information regarding types of Home Health
Agency sub-units will also be collected. Other than the information
above, new data being collected in this revision package is information
on, if applicable, where the supplier stores its patient records
electronically.
Form Number: CMS-855A (OCN: 0938-0685); Frequency: Annually;
Affected Public: State, Local, or Tribal governments; Number of
Respondents: 18,000; Number of Responses: 18,000; Total Annual Hours:
78,000. (For policy questions regarding this collection, contact Kim
McPhillips at 410-786-5374.)
Dated: November 8, 2013.
Martique Jones,
Deputy Director, Regulations Development Group, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2013-27305 Filed 11-14-13; 8:45 am]
BILLING CODE 4120-01-P