Federal Register Notice

17460

Federal Register / Vol. 81, No. 60 / Tuesday, March 29, 2016 / Notices
ACTION:

enhance/improve existing functions,
share data across federal agencies and
more efficiently utilize existing
applications.

SUMMARY:

Use of Data To Provide Effective
Outcomes/Weight 20%
The solution displays in a way that is
easy to understand, visually appealing,
and will help drive understanding of
current trends as well as
recommendations.
Creativity/Innovation/Weight 10%
The solution exceeds any internal
capability that GSA has for analysis of
data through its incorporation of
creative design elements and innovative
capabilities.
Valuable Information & Insights
Regarding Data/Weight 20%
The solver provides recommendations
for additional data elements to be
collected by the Federal Government.
The solver identifies gaps in the data
and utilizes external data sources and
research to aid the government in
setting future data collection policies.
Challenge Objectives:
• Utilize data to create an application,
API, and/or data mashup.
• Provide a better understanding of
use and needs of current and future data
assets.
• Post all open source solutions on
the GSA open source code site for future
use by the Federal Government
developer community and GSA.
All participants are required to check
in with Security upon arriving at the
GSA Central Office Building. Follow the
posted signs to the Conference Center,
Rooms 1459, 1460, and 1461.
All participants must sign the
document titled: Gratuitous Service
Agreement.
Dated: March 23, 2016.
Kris Rowley,
Director, Enterprise Information & Data
Mgmt. Ofc.
[FR Doc. 2016–07032 Filed 3–28–16; 8:45 am]
BILLING CODE 6820–34–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

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Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10615]

Emergency Clearance: Public
Information Collection Requirements
Submitted to the Office of Management
and Budget (OMB)
AGENCY:

Centers for Medicare &
Medicaid Services, HHS.

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Notice.

The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on an information collection
concerning CMS’ Healthy Indiana
Program (HIP) 2.0 Beneficiaries Survey.
We are also announcing that the
proposed information collection had
been submitted to OMB and was
approved under control number 0938–
1300 through September 30, 2016. In
accordance with the implementing
regulations of the Paperwork Reduction
Act of 1995 (PRA) at 5 CFR 1320.13, our
information collection request (ICR) was
submitted to OMB for emergency
processing. We requested emergency
review under 5 CFR 1320.13(a)(2)(i)
because public harm is reasonably likely
to result if the normal clearance
procedures were followed.
Following the regular PRA clearance
process would jeopardize the timely
completion of CMS’ evaluation of the
State’s upcoming non-emergency
medical transportation (NEMT) waiver
and other important waivers. Most
importantly, it would potentially cause
significant harm by depriving Medicaid
beneficiaries—especially those affected
by the NEMT waiver—of appropriate
medical services and needed care.
Although we have already received
OMB approval to test and develop the
survey instruments, we are soliciting
public comment during the testing and
development phase to meet the
conditions of OMB’s Terms of
Clearance. Importantly, CMS will
provide the public with another
opportunity to comment, via a 30-day
public comment period, prior to the
implementation phase of this effort.
Under the PRA, federal agencies are
required to publish notice in the
Federal Register concerning each
proposed ICR. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this ICR, including any of the following
subjects: (1) The necessity and utility of
the proposed ICR 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
April 8, 2016.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured

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consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to http://
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: CMS–10615/OMB Control
Number 0938–1300, 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
http://www.cms.hhs.gov/Paperwork
ReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
[email protected].
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 ICR. More detailed
information can be found in the
collection’s supporting statement and
associated materials (see ADDRESSES).
CMS–10615 Healthy Indiana Program
(HIP) 2.0 Beneficiaries Survey
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. In
compliance with the requirement of
section 3506(c)(2)(A) of the PRA, we
submitted to OMB the following
requirements for emergency approval.
OMB approved the emergency ICR on
March 21, 2016, with an expiration date
of September 30, 2016.

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17461

Federal Register / Vol. 81, No. 60 / Tuesday, March 29, 2016 / Notices
Information Collection
1. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Healthy Indiana
Program (HIP) 2.0 Beneficiaries Survey;
Use: Approval for testing and
developing the survey is vital to
adequately inform CMS decision
making regarding Section 1115 Waivers,
in particular the State’s upcoming
NEMT waiver due for renewal by
December 1, 2016. The NEMT benefit
provides transportation for Medicaid
beneficiaries who otherwise have no
means of transportation to get to and
from medical services. The Healthy
Indiana Program (HIP) 2.0
demonstration provides authority for
the State to not offer NEMT for the new
adult group during the first year of the
demonstration (except for pregnant
women and individuals determined to
be medically frail). CMS may extend the
State’s authority, subject to evaluation
of the impact of this policy on access to
care. Form Number: CMS–10615 (OMB
control number: 0938–1300); Frequency:
Once; Affected Public: Individuals and
households; Number of Respondents:
36; Total Annual Responses: 36; Total
Annual Hours: 36. (For policy questions
regarding this collection contact Teresa
DeCaro at 202–384–6309).
Written comments and
recommendations will be considered
from the public if received by the date
and address noted above.
Dated: March 22, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–06828 Filed 3–28–16; 8:45 am]
BILLING CODE 4120–01–P

FOR FURTHER INFORMATION CONTACT:

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration on Community Living
Proposed Information Collection
Activity; Comment Request; State
Developmental Disabilities Council 5Year State Plan
AGENCY:

Administration on Intellectual
and Developmental Disabilities,
Administration on Community Living,
HHS.
ACTION: Notice.
SUMMARY:

A plan developed by the State
Council on Developmental Disabilities
is required by federal statute. Each State
Council on Developmental Disabilities
must develop the plan, provide for
public comments in the State, provide
for approval by the State’s Governor,
and finally submit the plan on a fiveyear basis. On an annual basis, the
Council must review the plan and make
any amendments. The State Plan will be
used (1) by any amendments. The State
Plan will be used (2) by the Council as
a planning document; (3) by the
citizenry of the State as a mechanism for
commenting on the plans of the
Council; (4) by the Department as a
stewardship tool, for ensuring
compliance with the Developmental
Disabilities Assistance and Bill of Rights
Act, as one basis for providing technical
assistance (e.g., during site visits), and
as a support for management decision
making.

DATES:

Submit written comments on the
collection of information by May 31,
2016.

ADDRESSES:

Submit written comments
on the collection of information by
email to: [email protected].

Valerie Bond, Administration on
Community Living, Administration on
Intellectual and Developmental
Disabilities, Office of Program Support,
330 C Street SW., Room 1139–C,
Washington, DC 20201, (202) 795–7311.
SUPPLEMENTARY INFORMATION: In
compliance with the requirements of
Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration on Community Living is
soliciting public comment on the
specific aspects of the information
collection described above. Copies of
the proposed collection of information
can be obtained and comments may be
forwarded by writing to: Valerie Bond,
Administration on Community Living,
Administration on Intellectual and
Developmental Disabilities, Office of
Program Support, 330 C Street NW.,
Room 1139–C, Washington, DC 20201.
The Department specifically requests
comments on: (a) Whether the proposed
Collection of information is necessary
for the proper performance of the
function of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; (d) ways to
minimize the burden information to be
collected; and (e) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection technique
comments and or other forms of
information technology. Consideration
will be given to comments and
suggestions submitted within 60 days of
this publication.
Respondents: 56 State Developmental
Disabilities Councils.

ANNUAL BURDEN ESTIMATES
Number of
respondents

Instrument

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State Developmental Disabilities Council 5-Year State Plan ..........................

56

Estimated Total Annual Burden
Hours: 20,552.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

Dated: March 22, 2016.
Kathy Greenlee,
Administrator and Assistant Secretary for
Aging.

Food and Drug Administration

[FR Doc. 2016–07065 Filed 3–28–16; 8:45 am]
BILLING CODE 4154–01–P

[Docket No. FDA–2015–N–3037]

Pediatric Studies of Lorazepam;
Establishment of Public Docket
AGENCY:

Food and Drug Administration,

HHS.

ACTION:

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Notice; establishment of docket.

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Number of
responses per
respondent
1

Average
burden hours
per response
367

Total burden
hours
20,552

SUMMARY:

The Food and Drug
Administration (FDA) is establishing a
public docket to make available to the
public a report of the pediatric studies
of Lorazepam that were conducted in
accordance with the Public Health
Service Act (PHS Act) and submitted to
the Director of the National Institutes of
Health (NIH) and the Commissioner of
Food and Drugs.

DATES:

Submit either electronic or
written comments by April 28, 2016.

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