Submission for OMB Review; Comment Request, 17168-17169 [2016-06915]
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17168
Federal Register / Vol. 81, No. 59 / Monday, March 28, 2016 / Notices
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 (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-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 that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Medicaid and
CHIP Program (MACPro); Use: The
MACPro system is being transitioned to
become the system of record that will be
used by both state and CMS officials to:
Improve the state application and
federal review processes, improve
federal program management of
Medicaid programs and CHIP, and
standardize Medicaid program data.
Specifically, it will be used by state
agencies to: Submit and amend
Medicaid state plans, CHIP state plans
and ADPs (Information System
Advanced Planning Documents); submit
applications and amendments for state
waivers, demonstrations, and
benchmark and grant programs; and
submit reporting data.
Among the collections submitted for
approval under MACPro will be
relevant collections that are currently
approved under our generic umbrella
information collection request (CMS–
10398; OMB control number 0938–
1148), certain collections approved as a
regular stand-alone information
collections, and upcoming collections.
A list of those collections is included in
our PRA package.
While currently approved by OMB
under the regular PRA process which
requires 60- and 30-day comment
periods, CMS is proposing to have the
umbrella of MACPro collections
approved under OMB’s generic process
which would—in most cases—eliminate
the need for the 60- and 30-day
comment periods. Although the formal
60- and 30-day public comment periods
would be eliminated, the public may
continue to comment on any of the
MACPro collections at any time.
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Form Number: CMS–10434 (OMB
control number: 0938–1188); Frequency:
Monthly, yearly, quarterly, semiannually, once, or occasionally;
Affected Public: State, Local, or Tribal
Governments; Number of Respondents:
56; Total Annual Responses: 3,360;
Total Annual Hours: 96,844. (For policy
questions regarding this collection
contact Annette Pearson at 410–786–
6858).
Dated: March 23, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–06922 Filed 3–25–16; 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: Low Income Home Energy
Assistance Program 2015 RECS LIHEAP
Administrative Data Matching.
OMB No.: New Collection.
Description: The Low Income Home
Energy Assistance Program (LIHEAP)
block grant (42 U.S.C. 8621 et seq.) was
established under Title XXVI of the
Omnibus Budget Reconciliation Act of
1981, 97. The Office of Community
Services (OCS) within the U.S.
Department of Health and Human
Services (HHS), Administration for
Children and Families (ACF)
administers LIHEAP at the federal level.
The LIHEAP statute requires HHS to
report to Congress annually on program
impacts on recipient and eligible
households. The primary program goals,
as articulated in the statute, are to
ensure that benefits are targeted to those
households where the greatest program
impacts are expected, and to assure that
timely resources are available to
households experiencing home energy
crises.
OCS is seeking authorization to
collect data from all State LIHEAP
grantees and the District of Columbia
that will allow OCS to identify LIHEAP
recipients that responded to the
Residential Energy Consumption Survey
(RECS). The U.S. Energy Information
Administration (EIA) conducts this
survey to provide periodic national and
regional data on residential energy use
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Frm 00036
Fmt 4703
Sfmt 4703
in the United States. OCS uses RECS
data to furnish Congress and the
Administration with important national
and regional descriptive data on the
energy needs of low-income
households. Specific data elements OCS
is seeking to collect are detailed below.
State LIHEAP grantees will be asked
to furnish data for LIHEAP recipient
households that reside in areas included
in the RECS sample.
For each household, report the
following:
• Name
• Address (including ZIP code)
• Household or Client ID
• Telephone Number
• Household Size
• Gross Income
• Heating assistance awarded?
• Amount of heating assistance
• Date of heating assistance
• Cooling assistance awarded?
• Amount of cooling assistance
• Date of cooling assistance
• Crisis Assistance awarded?
• Amount of crisis assistance
• Date of crisis assistance
• Other Assistance awarded?
• Amount of other assistance
• Date of other assistance
• Presence of children 5 or younger
• Presence of adult 60 or older
• Presence of disabled
The following are additional optional
data items that grantees can provide if
the data are available in your database:
• Tenancy (i.e., own or rent)
• Type(s) of fuel used
• Heat included in rent
This data will help ACF to analyze
specific information for the LIHEAP
recipient population, including
information related to benefits targeting,
energy usage, and energy insecurity, and
it will support analysis of LIHEAP data
for the annual Report to Congress and
the annual LIHEAP Home Energy
Notebook.
Respondents: ACF published a
Federal Register notice on December 23,
2015 soliciting 60 days of public
comment on requiring State grantees to
provide household-level data for this
effort. ACF didn’t receive comments on
this notice.
Annual Burden Estimates
The table below shows the estimated
reporting burden for the RECS LIHEAP
administrative data matching effort.
These estimates are based on a small
number of interviews with grantees.
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17169
Federal Register / Vol. 81, No. 59 / Monday, March 28, 2016 / Notices
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Administrative data request .............................................................................
49
1
24
1,176
Estimated Total Annual Burden
Hours: 1,176.
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, 330 C Street SW.,
Washington, DC 20201. Attention
Reports Clearance Officer. All requests
should be identified by the title of the
information collection. Email address:
infocollection@acf.hhs.gov.
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
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, Attn:
Desk Officer for the Administration for
Children and Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2016–06915 Filed 3–25–16; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2016–N–0001]
Seventh Annual Predictive Safety
Testing Consortium/Food and Drug
Administration Scientific Workshop;
Public Workshop
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of public workshop.
The Food and Drug
Administration’s (FDA’s) Center for
Drug Evaluation and Research (CDER),
in cosponsorship with the Critical Path
Institute (C-Path), is announcing a
public scientific workshop to discuss
the impact of safety biomarkers on drug
development. The purpose of the
workshop is to discuss the following
Lhorne on DSK5TPTVN1PROD with NOTICES
SUMMARY:
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issues: Application of toxicometrics as a
translational safety strategy that
integrates nonclinical and clinical safety
approaches; uses of rodent and nonrodent nonclinical species in biomarker
qualification; and assay validation
aspects during biomarker development
and qualification.
DATES: The public workshop will be
held on April 25, 2016, from 8:30 a.m.
to 5 p.m.
ADDRESSES: The public workshop will
be held at the FDA White Oak Campus,
10903 New Hampshire Ave., Bldg. 31
Conference Center, the Great Room (Rm.
1503 A/B), Silver Spring, MD 20993–
0002.
The FDA Conference Center is a
federal facility and is located on the
White Oak campus and like all federal
facilities employs security procedures.
Entrance for scientific workshop
participants (non-FDA employees) is
through Building 1, where routine
security check procedures will be
performed. For parking and security
information, please refer to https://
www.fda.gov/AboutFDA/
WorkingatFDA/BuildingsandFacilities/
WhiteOakCampusInformation/
ucm241740.htm.
FOR FURTHER INFORMATION CONTACT:
Jacqueline Brooks-Leighton, Food and
Drug Administration, Center for Drug
Evaluation and Research, 10903 New
Hampshire Ave., Bldg. 21, Rm. 4521,
Silver Spring, MD 20993, 240–402–
5292, FAX: 301–796–9907, email:
jacqueline.brooks-leighton,@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
FDA and C-Path have expressed a
willingness to leverage their combined
strengths to develop and apply
predictive safety testing biomarkers in
drug development. This annual public
workshop is intended to bring together
leading academic experts, interested
pharmaceutical companies, regulatory
agencies, patient advocacy groups, and
non-profit organizations.
This meeting will offer the
opportunity to provide updates on the
progress made in various biomarker
development areas by the Predictive
Safety Testing Consortium, and to
discuss issues related to the regulatory
aspects of qualification and uptake of
biomarkers in drug development, as
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well as roadblocks to the sharing of
biomarker data by the scientific
community.
II. Attendance, Registration, and
Accommodations
There is no fee to attend the meeting,
but attendees must register in advance.
Space is limited, and registration will be
on a first-come, first-served basis. Onsite
registration on the day of the workshop
is not guaranteed but may be possible if
space is available. For questions
regarding registration, please contact
Stephanie Codd Anderson, 520–647–
8376, email: scanderson@gmail.com, at
the Critical Path Institute.
Persons interested in attending this
meeting in person must register online
by April 11, 2016 at https://
www.cvent.com/d/2fqzl2/4W.
FDA has verified the Web address, but
is not responsible for subsequent
changes to the Web site after this
document publishes in the Federal
Register. Interested persons without
Internet access should contact
Stephanie Codd Anderson at 520–647–
8376 to register.
The public workshop will also be
available to be viewed online via
webcast at https://collaboration.fda.gov/
pstc0416/.
Workshop attendees with special
needs due to a disability should contact
Stephanie Codd Anderson, 520–647–
8376, email: scanderson@gmail.com, at
the Critical Path Institute at least 7 days
before the scientific workshop.
Attendees are responsible for their
own hotel accommodations.
There will not be a transcript for this
meeting.
Dated: March 22, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016–06889 Filed 3–25–16; 8:45 am]
BILLING CODE 4164–01–P
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Agencies
[Federal Register Volume 81, Number 59 (Monday, March 28, 2016)]
[Notices]
[Pages 17168-17169]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-06915]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Low Income Home Energy Assistance Program 2015 RECS LIHEAP
Administrative Data Matching.
OMB No.: New Collection.
Description: The Low Income Home Energy Assistance Program (LIHEAP)
block grant (42 U.S.C. 8621 et seq.) was established under Title XXVI
of the Omnibus Budget Reconciliation Act of 1981, 97. The Office of
Community Services (OCS) within the U.S. Department of Health and Human
Services (HHS), Administration for Children and Families (ACF)
administers LIHEAP at the federal level.
The LIHEAP statute requires HHS to report to Congress annually on
program impacts on recipient and eligible households. The primary
program goals, as articulated in the statute, are to ensure that
benefits are targeted to those households where the greatest program
impacts are expected, and to assure that timely resources are available
to households experiencing home energy crises.
OCS is seeking authorization to collect data from all State LIHEAP
grantees and the District of Columbia that will allow OCS to identify
LIHEAP recipients that responded to the Residential Energy Consumption
Survey (RECS). The U.S. Energy Information Administration (EIA)
conducts this survey to provide periodic national and regional data on
residential energy use in the United States. OCS uses RECS data to
furnish Congress and the Administration with important national and
regional descriptive data on the energy needs of low-income households.
Specific data elements OCS is seeking to collect are detailed below.
State LIHEAP grantees will be asked to furnish data for LIHEAP
recipient households that reside in areas included in the RECS sample.
For each household, report the following:
Name
Address (including ZIP code)
Household or Client ID
Telephone Number
Household Size
Gross Income
Heating assistance awarded?
Amount of heating assistance
Date of heating assistance
Cooling assistance awarded?
Amount of cooling assistance
Date of cooling assistance
Crisis Assistance awarded?
Amount of crisis assistance
Date of crisis assistance
Other Assistance awarded?
Amount of other assistance
Date of other assistance
Presence of children 5 or younger
Presence of adult 60 or older
Presence of disabled
The following are additional optional data items that grantees can
provide if the data are available in your database:
Tenancy (i.e., own or rent)
Type(s) of fuel used
Heat included in rent
This data will help ACF to analyze specific information for the
LIHEAP recipient population, including information related to benefits
targeting, energy usage, and energy insecurity, and it will support
analysis of LIHEAP data for the annual Report to Congress and the
annual LIHEAP Home Energy Notebook.
Respondents: ACF published a Federal Register notice on December
23, 2015 soliciting 60 days of public comment on requiring State
grantees to provide household-level data for this effort. ACF didn't
receive comments on this notice.
Annual Burden Estimates
The table below shows the estimated reporting burden for the RECS
LIHEAP administrative data matching effort. These estimates are based
on a small number of interviews with grantees.
[[Page 17169]]
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Administrative data request................. 49 1 24 1,176
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 1,176.
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, 330 C Street SW., Washington, DC 20201. Attention
Reports Clearance Officer. All requests should be identified by the
title of the information collection. Email address:
infocollection@acf.hhs.gov.
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 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, Attn: Desk Officer for the Administration
for Children and Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2016-06915 Filed 3-25-16; 8:45 am]
BILLING CODE 4184-01-P