Agency Information Collection Activities: Proposed Collection; Comment Request, 62534-62536 [2015-26390]
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srobinson on DSK5SPTVN1PROD with NOTICES
62534
Federal Register / Vol. 80, No. 200 / Friday, October 16, 2015 / Notices
the Superfund Amendments and
Reauthorization Act of 1986 (SARA),
§ 104(i)(3), (42 U.S.C. 9604(i)(3)), directs
the ATSDR Administrator to prepare
Toxicological Profiles of Priority
hazardous substances and, as necessary,
to revise and publish each updated
toxicological profile.
Comments can include additional
information or reports on studies about
the health effects of Set 27 substances.
Although ATSDR considered key
studies for each of these substances
during the profile development process,
the Federal Register notice solicits any
relevant, additional studies, particularly
unpublished data. ATSDR will evaluate
the quality and relevance of such data
or studies for possible inclusion into the
profile. ATSDR remains committed to
providing a public comment period for
this document as a means to best serve
public health and our clients.
DATES: Written comments on this draft
Toxicological Profile must be received
on or before January 14, 2016.
ADDRESSES: You may submit comments,
identified by docket number ATSDR–
2015–0002, by any of the following
methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Division of Toxicology and
Human Health Sciences, Agency for
Toxic Substances and Disease Registry,
1600 Clifton Rd. NE., MS F–57, Atlanta,
GA 30329. Attn: Docket No. ATSDR–
2015–0002.
Instructions: All submissions received
must include the agency name and
docket number for this notice. All
relevant comments will be posted
without change. Because all public
comments regarding ATSDR
Toxicological Profiles are available for
public inspection, no confidential
business information or other
confidential information should be
submitted in response to this notice.
FOR FURTHER INFORMATION CONTACT: Ms.
Delores Grant, Division of Toxicology
and Human Health Sciences, Agency for
Toxic Substances and Disease Registry,
1600 Clifton Rd. NE., MS F–57, Atlanta,
GA 30329. Phone: (800) 232–4636 or
770–488–3351.
SUPPLEMENTARY INFORMATION: The
Superfund Amendments and
Reauthorization Act (SARA) (Pub. L.
99–499) amends the Comprehensive
Environmental Response,
Compensation, and Liability Act
(CERCLA or Superfund) (42 U.S.C. 9601
et seq.) by establishing certain
responsibilities for ATSDR and the U.S.
Environmental Protection Agency (U.S.
EPA) regarding hazardous substances
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18:54 Oct 15, 2015
Jkt 238001
most commonly found at facilities on
the CERCLA National Priorities List
(NPL). As part of these responsibilities,
the ATSDR Administrator must prepare
Toxicological Profiles for substances
enumerated on the priority list of
hazardous substances. This list
identifies 275 hazardous substances
which, according to ATSDR and U.S.
EPA, pose the most significant potential
threat to human health. The availability
of the revised priority list of 275
hazardous substances was announced in
the Federal Register on May 28, 2014
(79 FR 30613). In addition, ATSDR has
the authority to prepare Toxicological
Profiles for substances not found at sites
on the National Priorities List, in an
effort to ‘‘. . . establish and maintain
inventory of literature, research, and
studies on the health effects of toxic
substances’’ under CERCLA Section
104(i)(1)(B). ATSDR also prepares
Toxicological Profiles in response to
requests for consultation under section
104(i)(4), and as otherwise necessary to
support the site-specific response
actions conducted by ATSDR.
Each profile will include an
examination, a summary, and an
interpretation of available toxicological
information and epidemiological
evaluations. This information and these
data identify the levels of significant
human exposure for the substance and
for the associated health effects. The
profiles must also include a
determination of whether adequate
information on the health effects of each
substance is available (or in the process
of development) in order to identify
levels of significant human exposure. If
adequate information is not available,
ATSDR, in cooperation with the
National Toxicology Program (NTP), is
required to ensure the initiation of a
program of research to provide such
information.
SET 27 TOXICOLOGICAL PROFILES
Name
1 ..
2 ..
3 ..
4 ..
5 ..
Polybrominated
Biphenyl
Ethers
(PBDEs) UPDATE.
N,N-Diethyl-meta-toluamide (DEET).
Toluene Diisocyanates (mixture).
Methylenediphenyl
Diisocyanates
(NEW).
Nitrates/Nitrites (NEW).
Toluene (UPDATE).
The Set 27 Toxicological Profiles are
available online at https://
www.atsdr.cdc.gov/toxprofiles/
index.asp and https://
PO 00000
Frm 00022
Fmt 4703
Sfmt 4703
www.regulations.gov, Docket No.
ATSDR–2015–0002.
Donna B. Knutson,
Acting Director, Office of Policy, Planning
and Evaluation, National Center for
Environmental Health and Agency for Toxic
Substances and Disease Registry.
[FR Doc. 2015–26321 Filed 10–15–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10003, CMS–
10467, CMS–1450(UB–04), CMS–1500(08–
05)]
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
December 15, 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
DATES:
E:\FR\FM\16OCN1.SGM
16OCN1
Federal Register / Vol. 80, No. 200 / Friday, October 16, 2015 / Notices
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 ll,
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:
srobinson on DSK5SPTVN1PROD with NOTICES
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–10003 Notice of Denial of Medical
Coverage (or Payment)
CMS–10467 Evaluation of the Graduate
Nurse Education Demonstration
Program
CMS–1450(UB–04) Medicare Uniform
Institutional Provider Bill and
Supporting Regulations CMS–
1500(08–05) Health Insurance
Common Claims Form and
Supporting Regulations
Under 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
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18:54 Oct 15, 2015
Jkt 238001
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 Collection
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Notice of Denial
of Medical Coverage (or Payment); Use:
Medicare health plans, including
Medicare Advantage plans, cost plans,
and Health Care Prepayment Plans, are
required to issue the CMS–10003 form
when a request for either a medical
service or payment is denied in whole
or in part. The notice explains why the
plan denied the service or payment and
informs Medicare enrollees of their
appeal rights. The notice is also used, as
appropriate, to explain Medicaid appeal
rights to full dual eligible individuals
enrolled in a Medicare health plan that
is also managing the individual’s
Medicaid benefits. To that end, the
revised notice contains bracketed text
the plan will insert if the denial notice
is being delivered to an enrollee who is
a full dual eligible. The text in square
brackets ‘‘[ ]’’ reflects the Federal
protections for Medicaid managed care
enrollees. Since a State may offer
additional protections, there is also freetext space for inclusion of any Statespecific protections that exceed the
Federal protections. Form Number:
CMS–10003 (OMB control number:
0938–0829). Frequency: Occasionally;
Affected Public: Private sector (Business
or other for-profit and Not-for-profit
institutions); Number of Respondents:
730; Total Annual Responses:
33,574,293; Total Annual Hours:
5,593,477. (For policy questions
regarding this collection contact Staci
Paige at 410–786–2045. For all other
issues call 410–786–1326.)
2. Type of Information Collection
Request: Revision of a currently
approved information collection; Title
of Information Collection: Evaluation of
the Graduate Nurse Education
Demonstration Program; Use: The
Graduate Nurse Education (GNE)
Demonstration is mandated under
Section 5509 of the Affordable Care Act
(ACA) under title XVIII of the Social
Security Act (42 U.S.C. 1395 et seq.).
According to Section 5509 of the ACA,
the five selected demonstration sites
receive ‘‘payment for the hospital’s
reasonable costs for the provision of
qualified clinical training to advance
PO 00000
Frm 00023
Fmt 4703
Sfmt 4703
62535
practice registered nurses.’’ Section
5509 of the ACA also states that an
evaluation of the graduate nurse
education demonstration must be
completed no later than October 17,
2017. This evaluation includes analysis
of the following: (1) Growth in the
number of advanced practice registered
nurses (APRNs) with respect to a
specific base year as a result of the
demonstration; (2) growth for each of
the following specialties: clinical nurse
specialist, nurse practitioner, certified
nurse anesthetist, certified nursemidwife; and (3) costs to the Medicare
program as result of the demonstration.
All information collected through the
Evaluation of the GNE project will be
used to meet the requirements specified
under the ACA Section 5509. We will
also use the information to determine
the overall effectiveness of the GNE
project. The process evaluation seeks to
understand how the demonstration is
implemented overall, how that
implementation has changed over time,
which aspects of the demonstration
have been successful or unsuccessful,
and what plans the sites have for the
remainder of the implementation and
after the demonstration formally ends.
The process evaluation will answer both
quantitative and qualitative questions.
Form Number: CMS–10467 (OMB
control number: 0938–1212); Frequency:
Annually; Affected Public: State, Local,
or Tribal Governments; Private sector
(Business and other for-profit and Notfor-profit institutions); Number of
Respondents: 104; Total Annual
Responses: 104; Total Annual Hours:
802. (For policy questions regarding this
collection contact Pauline KarikariMartin at 410–786–1040.)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Medicare
Uniform Institutional Provider Bill and
Supporting Regulations in 42 CFR
424.5; Use: Section 42 CFR 424.5(a)(5)
requires providers of services to submit
a claim for payment prior to any
Medicare reimbursement. Charges billed
are coded by revenue codes. The bill
specifies diagnoses according to the
International Classification of Diseases,
Ninth Edition (ICD–9–CM) code.
Inpatient procedures are identified by
ICD–9–CM codes, and outpatient
procedures are described using the CMS
Common Procedure Coding System
(HCPCS). These are standard systems of
identification for all major health
insurance claims payers. Submission of
information on the CMS–1450 permits
Medicare intermediaries to receive
consistent data for proper payment.
Form Numbers: CMS–1450 (UB–04)
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62536
Federal Register / Vol. 80, No. 200 / Friday, October 16, 2015 / Notices
(OMB control number: 0938–0997);
Frequency: On occasion; Affected
Public: Private sector (Business or other
for-profit and Not-for-profit
institutions); Number of Respondents:
53,111; Total Annual Responses:
181,909,654; Total Annual Hours:
1,567,455. (For policy questions
regarding this collection contact Matt
Klischer at 410–786–7488.)
4. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Health
Insurance Common Claims Form and
Supporting Regulations at 42 CFR part
424, Subpart C; Use: The Form CMS–
1500 answers the needs of many health
insurers. It is the basic form prescribed
by CMS for the Medicare program for
claims from physicians and suppliers.
The Medicaid State Agencies,
CHAMPUS/TriCare, Blue Cross/Blue
Shield Plans, the Federal Employees
Health Benefit Plan, and several private
health plans also use it; it is the de facto
standard ‘‘professional’’ claim form.
Medicare carriers use the data
collected on the CMS–1500 and the
CMS–1490S to determine the proper
amount of reimbursement for Part B
medical and other health services (as
listed in section 1861(s) of the Social
Security Act) provided by physicians
and suppliers to beneficiaries. The
CMS–1500 is submitted by physicians/
suppliers for all Part B Medicare.
Serving as a common claim form, the
CMS–1500 can be used by other thirdparty payers (commercial and nonprofit
health insurers) and other Federal
programs (e.g., CHAMPUS/TriCare,
Railroad Retirement Board (RRB), and
Medicaid). However, as the CMS–1500
displays data items required for other
third-party payers in addition to
Medicare, the form is considered too
complex for use by beneficiaries when
they file their own claims. Therefore,
the CMS–1490S (Patient’s Request for
Medicare Payment) was explicitly
developed for easy use by beneficiaries
who file their own claims. The form can
be obtained from any Social Security
office or Medicare carrier. Form
Number: CMS–1500(08/05), CMS–1490–
S (OMB control number: 0938–0999)
Frequency: On occasion; Affected
Public: State, Local, or Tribal
Governments, Private sector (Business
or other-for-profit and Not-for-profit
institutions); Number of Respondents:
1,448,346; Total Annual Responses:
988,005,045; Total Annual Hours:
21,418,336. (For policy questions
regarding this collection contact
Shannon Seales at 410–786–4089.)
Dated: October 13, 2015.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2015–26390 Filed 10–15–15; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Native Language Preservation
and Maintenance Grant Application
Template Pilot (Funding Application
Submission Tool (F.A.S.T. form))
OMB No.:
Description: The proposed F.A.S.T.
form is intended to be used by
applicants in the Administration for
Native Americans’ Native American
Language Preservation and Maintenance
grant competition in FY 2016. The
F.A.S.T. form is proposed to be piloted
as a consolidated and streamlined pre-
formatted electronic application form
that is user-friendly and has an
interactive interface providing structure
and clarity for applicants. The proposed
F.A.S.T. form is not intended to replace
the Funding Opportunity
Announcement (FOAs) which will still
function as the full text of all funding
opportunities for which applications are
sought and considered by the
Administration for Native Americans.
The proposed F.A.S.T. form will be
used in a pilot capacity in just one
Administration for Native Americans’
discretionary program areas: Native
American Language Preservation and
Maintenance. All applicants applying
for funding in that program area will be
required to use the F.A.S.T. form during
the pilot competition proposed for FY16
unless they request and receive
approval to submit a paper application.
By using the F.A.S.T. form no applicant
will be required to provide any
information beyond what is already
required by the FOA. Additionally, free
training and technical assistance will be
available to all applicants on use of the
F.A.S.T. form.
ANA intends to use the project
proposals submitted via the F.A.S.T.
form to make funding decisions for
Native American Language Preservation
and Maintenance grant awards made in
the FY 2016 pilot year. In addition,
ANA will solicit feedback from
applicants and panel reviewers to obtain
feedback on the results, outcomes, and
their recommendations regarding the
F.A.S.T. form as a user friendly method
of applying for funding opportunities. If
the pilot is successful in making it
easier for applicants to apply, ANA will
consider potentially expanding use of
the F.A.S.T. form to all Administration
for Native Americans’ discretionary
funding areas in subsequent years.
Respondents: 40.
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
F.A.S.T. form ...................................................................................................
40
28
.50
14
Attn: ACF Reports Clearance Officer. All
requests should be identified by the title
of the information collection. Email
address: infocollection@acf.hhs.gov.
srobinson on DSK5SPTVN1PROD with NOTICES
Estimated Total Annual Burden
Hours: 560.
Additional Information
Copies of the proposed collection may
be obtained by writing to the
Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
VerDate Sep<11>2014
18:54 Oct 15, 2015
Jkt 238001
OMB Comment
OMB is required to make a decision
concerning the collection of information
between 30 and 60 days after
publication of this document in the
PO 00000
Frm 00024
Fmt 4703
Sfmt 4703
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication. Written comments and
recommendations for the proposed
information collection should be sent
directly to the following: Office of
Management and Budget, Paperwork
Reduction Project, Email:
OIRA_SUBMISSION@OMB.EOP.GOV,
E:\FR\FM\16OCN1.SGM
16OCN1
Agencies
[Federal Register Volume 80, Number 200 (Friday, October 16, 2015)]
[Notices]
[Pages 62534-62536]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-26390]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10003, CMS-10467, CMS-1450(UB-04), CMS-
1500(08-05)]
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 December 15, 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
[[Page 62535]]
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-10003 Notice of Denial of Medical Coverage (or Payment)
CMS-10467 Evaluation of the Graduate Nurse Education Demonstration
Program
CMS-1450(UB-04) Medicare Uniform Institutional Provider Bill and
Supporting Regulations CMS-1500(08-05) Health Insurance Common Claims
Form and Supporting Regulations
Under 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 Collection
1. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Notice of Denial
of Medical Coverage (or Payment); Use: Medicare health plans, including
Medicare Advantage plans, cost plans, and Health Care Prepayment Plans,
are required to issue the CMS-10003 form when a request for either a
medical service or payment is denied in whole or in part. The notice
explains why the plan denied the service or payment and informs
Medicare enrollees of their appeal rights. The notice is also used, as
appropriate, to explain Medicaid appeal rights to full dual eligible
individuals enrolled in a Medicare health plan that is also managing
the individual's Medicaid benefits. To that end, the revised notice
contains bracketed text the plan will insert if the denial notice is
being delivered to an enrollee who is a full dual eligible. The text in
square brackets ``[ ]'' reflects the Federal protections for Medicaid
managed care enrollees. Since a State may offer additional protections,
there is also free-text space for inclusion of any State-specific
protections that exceed the Federal protections. Form Number: CMS-10003
(OMB control number: 0938-0829). Frequency: Occasionally; Affected
Public: Private sector (Business or other for-profit and Not-for-profit
institutions); Number of Respondents: 730; Total Annual Responses:
33,574,293; Total Annual Hours: 5,593,477. (For policy questions
regarding this collection contact Staci Paige at 410-786-2045. For all
other issues call 410-786-1326.)
2. Type of Information Collection Request: Revision of a currently
approved information collection; Title of Information Collection:
Evaluation of the Graduate Nurse Education Demonstration Program; Use:
The Graduate Nurse Education (GNE) Demonstration is mandated under
Section 5509 of the Affordable Care Act (ACA) under title XVIII of the
Social Security Act (42 U.S.C. 1395 et seq.). According to Section 5509
of the ACA, the five selected demonstration sites receive ``payment for
the hospital's reasonable costs for the provision of qualified clinical
training to advance practice registered nurses.'' Section 5509 of the
ACA also states that an evaluation of the graduate nurse education
demonstration must be completed no later than October 17, 2017. This
evaluation includes analysis of the following: (1) Growth in the number
of advanced practice registered nurses (APRNs) with respect to a
specific base year as a result of the demonstration; (2) growth for
each of the following specialties: clinical nurse specialist, nurse
practitioner, certified nurse anesthetist, certified nurse-midwife; and
(3) costs to the Medicare program as result of the demonstration.
All information collected through the Evaluation of the GNE project
will be used to meet the requirements specified under the ACA Section
5509. We will also use the information to determine the overall
effectiveness of the GNE project. The process evaluation seeks to
understand how the demonstration is implemented overall, how that
implementation has changed over time, which aspects of the
demonstration have been successful or unsuccessful, and what plans the
sites have for the remainder of the implementation and after the
demonstration formally ends. The process evaluation will answer both
quantitative and qualitative questions. Form Number: CMS-10467 (OMB
control number: 0938-1212); Frequency: Annually; Affected Public:
State, Local, or Tribal Governments; Private sector (Business and other
for-profit and Not-for-profit institutions); Number of Respondents:
104; Total Annual Responses: 104; Total Annual Hours: 802. (For policy
questions regarding this collection contact Pauline Karikari-Martin at
410-786-1040.)
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Medicare Uniform
Institutional Provider Bill and Supporting Regulations in 42 CFR 424.5;
Use: Section 42 CFR 424.5(a)(5) requires providers of services to
submit a claim for payment prior to any Medicare reimbursement. Charges
billed are coded by revenue codes. The bill specifies diagnoses
according to the International Classification of Diseases, Ninth
Edition (ICD-9-CM) code. Inpatient procedures are identified by ICD-9-
CM codes, and outpatient procedures are described using the CMS Common
Procedure Coding System (HCPCS). These are standard systems of
identification for all major health insurance claims payers. Submission
of information on the CMS-1450 permits Medicare intermediaries to
receive consistent data for proper payment. Form Numbers: CMS-1450 (UB-
04)
[[Page 62536]]
(OMB control number: 0938-0997); Frequency: On occasion; Affected
Public: Private sector (Business or other for-profit and Not-for-profit
institutions); Number of Respondents: 53,111; Total Annual Responses:
181,909,654; Total Annual Hours: 1,567,455. (For policy questions
regarding this collection contact Matt Klischer at 410-786-7488.)
4. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Health Insurance
Common Claims Form and Supporting Regulations at 42 CFR part 424,
Subpart C; Use: The Form CMS-1500 answers the needs of many health
insurers. It is the basic form prescribed by CMS for the Medicare
program for claims from physicians and suppliers. The Medicaid State
Agencies, CHAMPUS/TriCare, Blue Cross/Blue Shield Plans, the Federal
Employees Health Benefit Plan, and several private health plans also
use it; it is the de facto standard ``professional'' claim form.
Medicare carriers use the data collected on the CMS-1500 and the
CMS-1490S to determine the proper amount of reimbursement for Part B
medical and other health services (as listed in section 1861(s) of the
Social Security Act) provided by physicians and suppliers to
beneficiaries. The CMS-1500 is submitted by physicians/suppliers for
all Part B Medicare. Serving as a common claim form, the CMS-1500 can
be used by other third-party payers (commercial and nonprofit health
insurers) and other Federal programs (e.g., CHAMPUS/TriCare, Railroad
Retirement Board (RRB), and Medicaid). However, as the CMS-1500
displays data items required for other third-party payers in addition
to Medicare, the form is considered too complex for use by
beneficiaries when they file their own claims. Therefore, the CMS-1490S
(Patient's Request for Medicare Payment) was explicitly developed for
easy use by beneficiaries who file their own claims. The form can be
obtained from any Social Security office or Medicare carrier. Form
Number: CMS-1500(08/05), CMS-1490-S (OMB control number: 0938-0999)
Frequency: On occasion; Affected Public: State, Local, or Tribal
Governments, Private sector (Business or other-for-profit and Not-for-
profit institutions); Number of Respondents: 1,448,346; Total Annual
Responses: 988,005,045; Total Annual Hours: 21,418,336. (For policy
questions regarding this collection contact Shannon Seales at 410-786-
4089.)
Dated: October 13, 2015.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2015-26390 Filed 10-15-15; 8:45 am]
BILLING CODE 4120-01-P