Proposed Information Collection Activity; Comment Request; State Developmental Disabilities Council 5-Year State Plan, 17461 [2016-07065]
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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: Valerie.Bond@acl.hhs.gov.
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
State Developmental Disabilities Council 5-Year State Plan ..........................
56
mstockstill on DSK4VPTVN1PROD with NOTICES
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:
VerDate Sep<11>2014
19:43 Mar 28, 2016
Jkt 238001
PO 00000
Notice; establishment of docket.
Frm 00037
Fmt 4703
Sfmt 4703
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.
E:\FR\FM\29MRN1.SGM
29MRN1
]]>Agencies
[Federal Register Volume 81, Number 60 (Tuesday, March 29, 2016)]
[Notices]
[Page 17461]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-07065]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration on Community Living
Proposed Information Collection Activity; Comment Request; State
Developmental Disabilities Council 5-Year 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 five-year 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: Valerie.Bond@acl.hhs.gov.
FOR FURTHER INFORMATION CONTACT: 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 Average
Instrument Number of responses per burden hours Total burden
respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
State Developmental Disabilities Council 5-Year 56 1 367 20,552
State Plan.....................................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 20,552.
Dated: March 22, 2016.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2016-07065 Filed 3-28-16; 8:45 am]
BILLING CODE 4154-01-P
