Agency Information Collection Activities: Proposed Collection; Comment Request, 40105-40106 [2014-16076]
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Federal Register / Vol. 79, No. 133 / Friday, July 11, 2014 / Notices
Director of applications to be considered
for funding support; (4) review of
research portfolios, and (5) review of
program proposals.
Matters for Discussion: The Board of
Scientific Counselors, National Center
for Injury Prevention and Control (BSC,
NCIPC) will meet to conduct a
Secondary Peer Review of extramural
research grant applications received in
response to five (5) Funding
Opportunity Announcements (FOAs)
‘‘Research to Prevent Prescription Drug
Overdoses’’, FOA CE14–002; ‘‘Motor
Vehicle Injury Prevention: Evaluation of
Increased Nighttime Enforcement of
Seatbelts Uses’’, FOA CE14–003;
‘‘Research on Integration of Injury
Prevention in Health Systems’’, FOA
CE14–004; ‘‘Evaluating Promising
Strategies to Build the Evidence Base for
Sexual Violence Prevention’’, FOA
CE14–005; and ‘‘Research Grants for
Preventing Violence and ViolenceRelated Injury’’, FOA CE14–006.
Applications will be assessed for
applicability to the Center’s mission and
programmatic balance.
Recommendations from the secondary
review will be voted upon and the
applications will be forwarded to the
Acting Center Director for consideration
for funding support.
Contact Person for More Information:
Gwendolyn H. Cattledge, Ph.D.,
M.S.E.H., Deputy Associate Director for
Science, NCIPC, CDC, 4770 Buford
Highway NE., Mailstop F–63, Atlanta,
GA 30341, Telephone (770) 488–1430.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2014–16206 Filed 7–10–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10137, CMS–
10237, CMS–10398 and CMS–10522]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Department of
Health and Human 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
September 9, 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
DATES:
PO 00000
Frm 00048
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40105
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–10137 Solicitation for
Applications for Medicare Prescription
Drug Plan 2015 Contracts
CMS–10237 Part C—Medicare
Advantage and 1876 Cost Plan
Expansion Application
CMS–10398 Generic Clearance for
Medicaid and CHIP State Plan, Waiver,
and Program Submissions
CMS–10522 Executive Summary Form
for Research Identifiable Data
Under the Paperwork Reduction Act
(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.
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40106
Federal Register / Vol. 79, No. 133 / Friday, July 11, 2014 / Notices
Information Collection
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Solicitation for
Applications for Medicare Prescription
Drug Plan 2015 Contracts; Use: The
information will be collected under the
solicitation of proposals from PDP, MA–
PD, Cost Plan, PACE, and EGWP
applicants. We will use the information
to ensure that applicants meet our
requirements and support the
determination of contract awards.
Participation in the Part D program is
voluntary in nature. Only organizations
that are interested in participating in the
program will respond to the solicitation.
The MA–PDs that voluntarily
participate in the Part C program must
submit a Part D application and
successful bid. Form Number: CMS–
10137 (OMB control number: 0938—
0936); Frequency: Yearly; Affected
Public: Private sector—Business or other
for-profits and Not-for-profit
institutions; Number of Respondents:
254; Total Annual Responses: 254; Total
Annual Hours: 2,193. (For policy
questions regarding this collection
contact Arianne Spaccarelli at 410–786–
5715).
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Part C—
Medicare Advantage and 1876 Cost Plan
Expansion Application; Use: The
information will be collected under the
solicitation of Part C applications from
MA, EGWP Plan, and Cost Plan
applicants and will be used to ensure
that applicants meet our requirements
and support the determination of
contract awards. Participation in all
programs is voluntary in nature; only
organizations that are interested in
participating in the program will
respond to the solicitation. The MA–
PDs that voluntarily participate in the
Part C program must submit a Part D
application and successful bid. Form
Number: CMS–10237 (OMB control
number: 0938–0935); Frequency: Yearly;
Affected Public: Private sector—
Business or other for-profits and Notfor-profit institutions; Number of
Respondents: 566; Total Annual
Responses: 566; Total Annual Hours:
22,625. (For policy questions regarding
this collection contact Melissa Staud at
410–786–3669).
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Generic
Clearance for Medicaid and CHIP State
Plan, Waiver, and Program Submissions;
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Use: State Medicaid and CHIP agencies
are responsible for developing
submissions to CMS, including State
plan amendments and requests for
waivers and program demonstrations.
States use templates when they are
available and submit the forms to
review for consistency with statutory
and regulatory requirements (or in the
case of waivers and demonstrations
whether the proposal is likely to
promote the objectives of the Medicaid
program). If the requirements are met,
we approve the States’ submissions
giving the States the authority to
implement the flexibilities. For a State
to receive Medicaid Title XIX funding,
there must be an approved Title XIX
State plan.
The development of streamlined
submissions forms enhances the
collaboration and partnership between
States and CMS by documenting our
policy for States to use as they are
developing program changes.
Streamlined forms improve efficiency of
administration by creating a common
and user-friendly understanding of the
information we need to quickly process
requests for State plan amendments,
waivers, and demonstration, as well as
ongoing reporting. Form Number: CMS–
10398 (OMB control number: 0938–
1148); Frequency: Collection specific,
but generally the frequency is yearly,
once, and occasionally; Affected Public:
State, Local, or Tribal Governments;
Number of Respondents: 56; Total
Annual Responses: 1,120; Total Annual
Hours: 28,747. (For policy questions
regarding this collection contact
Annette Pearson at 410–786–6858).
4. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Executive
Summary Form for Research Identifiable
Data; Use: The Centers for Medicare &
Medicaid Services (CMS) is responsible
for administering the Medicare,
Medicaid and State Children’s Health
Insurance Programs. We collect data to
support the Agency’s mission and
operations. These data include
information about Medicare
beneficiaries, Medicare claims,
Medicare providers, and Medicaid
eligibility and claims. We disclose the
identifiable data consistent with the
routine uses identified in the Privacy
Act Systems of Records notices that are
published in the Federal Register and
the limitations on uses and disclosures
that are set out in the HIPAA Privacy
Rule.
All requests for identifiable data are
received and reviewed by the Division
of Privacy Operations & Compliance
(DPOC) in the Office of E-Health
PO 00000
Frm 00049
Fmt 4703
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Standards and Services. The DPOC staff
and the CMS Privacy Officer review the
requests to determine if there is legal
authorization for disclosure of the data.
If legal authorization exists, the request
is reviewed to ensure that the minimal
data necessary is requested and
approved for the project. Requests for
identifiable data for research purposes
must be submitted to and approved by
the CMS Privacy Board. To assist the
CMS Privacy Board with its review of
research data requests, OIPDA has
developed the Executive Summary (ES)
forms. The ES collects all the
information that the CMS Privacy Board
needs to review and make a
determination on whether the request
meets the requirements for release of
identifiable data for research purposes.
We currently have three versions of the
ES Form and an ES Supplement for
Requestors of the National Death Index
(NDI) Causes of Death Variables. Each
meets the need for a different type of
requestor. Form Number: CMS–10522
(OMB control number: 0938–New);
Frequency: On occasion; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
325; Total Annual Responses: 325; Total
Annual Hours: 650. (For policy
questions regarding this collection
contact Kim Elmo at 410–786–0161).
Dated: July 3, 2014.
Martique Jones,
Deputy Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2014–16076 Filed 7–10–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–304/CMS–304a,
CMS–368/CMS–R–144 and CMS–10517]
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
SUMMARY:
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Agencies
[Federal Register Volume 79, Number 133 (Friday, July 11, 2014)]
[Notices]
[Pages 40105-40106]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-16076]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10137, CMS-10237, CMS-10398 and CMS-10522]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Department of Health
and Human 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 September 9, 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-10137 Solicitation for Applications for Medicare Prescription Drug
Plan 2015 Contracts
CMS-10237 Part C--Medicare Advantage and 1876 Cost Plan Expansion
Application
CMS-10398 Generic Clearance for Medicaid and CHIP State Plan, Waiver,
and Program Submissions
CMS-10522 Executive Summary Form for Research Identifiable Data
Under the Paperwork Reduction Act (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.
[[Page 40106]]
Information Collection
1. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Solicitation for
Applications for Medicare Prescription Drug Plan 2015 Contracts; Use:
The information will be collected under the solicitation of proposals
from PDP, MA-PD, Cost Plan, PACE, and EGWP applicants. We will use the
information to ensure that applicants meet our requirements and support
the determination of contract awards. Participation in the Part D
program is voluntary in nature. Only organizations that are interested
in participating in the program will respond to the solicitation. The
MA-PDs that voluntarily participate in the Part C program must submit a
Part D application and successful bid. Form Number: CMS-10137 (OMB
control number: 0938--0936); Frequency: Yearly; Affected Public:
Private sector--Business or other for-profits and Not-for-profit
institutions; Number of Respondents: 254; Total Annual Responses: 254;
Total Annual Hours: 2,193. (For policy questions regarding this
collection contact Arianne Spaccarelli at 410-786-5715).
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Part C--Medicare
Advantage and 1876 Cost Plan Expansion Application; Use: The
information will be collected under the solicitation of Part C
applications from MA, EGWP Plan, and Cost Plan applicants and will be
used to ensure that applicants meet our requirements and support the
determination of contract awards. Participation in all programs is
voluntary in nature; only organizations that are interested in
participating in the program will respond to the solicitation. The MA-
PDs that voluntarily participate in the Part C program must submit a
Part D application and successful bid. Form Number: CMS-10237 (OMB
control number: 0938-0935); Frequency: Yearly; Affected Public: Private
sector--Business or other for-profits and Not-for-profit institutions;
Number of Respondents: 566; Total Annual Responses: 566; Total Annual
Hours: 22,625. (For policy questions regarding this collection contact
Melissa Staud at 410-786-3669).
3. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Generic Clearance
for Medicaid and CHIP State Plan, Waiver, and Program Submissions; Use:
State Medicaid and CHIP agencies are responsible for developing
submissions to CMS, including State plan amendments and requests for
waivers and program demonstrations. States use templates when they are
available and submit the forms to review for consistency with statutory
and regulatory requirements (or in the case of waivers and
demonstrations whether the proposal is likely to promote the objectives
of the Medicaid program). If the requirements are met, we approve the
States' submissions giving the States the authority to implement the
flexibilities. For a State to receive Medicaid Title XIX funding, there
must be an approved Title XIX State plan.
The development of streamlined submissions forms enhances the
collaboration and partnership between States and CMS by documenting our
policy for States to use as they are developing program changes.
Streamlined forms improve efficiency of administration by creating a
common and user-friendly understanding of the information we need to
quickly process requests for State plan amendments, waivers, and
demonstration, as well as ongoing reporting. Form Number: CMS-10398
(OMB control number: 0938-1148); Frequency: Collection specific, but
generally the frequency is yearly, once, and occasionally; Affected
Public: State, Local, or Tribal Governments; Number of Respondents: 56;
Total Annual Responses: 1,120; Total Annual Hours: 28,747. (For policy
questions regarding this collection contact Annette Pearson at 410-786-
6858).
4. Type of Information Collection Request: New collection (Request
for a new OMB control number); Title of Information Collection:
Executive Summary Form for Research Identifiable Data; Use: The Centers
for Medicare & Medicaid Services (CMS) is responsible for administering
the Medicare, Medicaid and State Children's Health Insurance Programs.
We collect data to support the Agency's mission and operations. These
data include information about Medicare beneficiaries, Medicare claims,
Medicare providers, and Medicaid eligibility and claims. We disclose
the identifiable data consistent with the routine uses identified in
the Privacy Act Systems of Records notices that are published in the
Federal Register and the limitations on uses and disclosures that are
set out in the HIPAA Privacy Rule.
All requests for identifiable data are received and reviewed by the
Division of Privacy Operations & Compliance (DPOC) in the Office of E-
Health Standards and Services. The DPOC staff and the CMS Privacy
Officer review the requests to determine if there is legal
authorization for disclosure of the data. If legal authorization
exists, the request is reviewed to ensure that the minimal data
necessary is requested and approved for the project. Requests for
identifiable data for research purposes must be submitted to and
approved by the CMS Privacy Board. To assist the CMS Privacy Board with
its review of research data requests, OIPDA has developed the Executive
Summary (ES) forms. The ES collects all the information that the CMS
Privacy Board needs to review and make a determination on whether the
request meets the requirements for release of identifiable data for
research purposes. We currently have three versions of the ES Form and
an ES Supplement for Requestors of the National Death Index (NDI)
Causes of Death Variables. Each meets the need for a different type of
requestor. Form Number: CMS-10522 (OMB control number: 0938-New);
Frequency: On occasion; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 325; Total Annual Responses: 325;
Total Annual Hours: 650. (For policy questions regarding this
collection contact Kim Elmo at 410-786-0161).
Dated: July 3, 2014.
Martique Jones,
Deputy Director, Regulations Development Group, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2014-16076 Filed 7-10-14; 8:45 am]
BILLING CODE 4120-01-P