Submission for OMB Review; Comment Request, 58311 [2013-22995]
Download as PDF
<![CDATA[
58311
Federal Register / Vol. 78, No. 184 / Monday, September 23, 2013 / Notices
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, Fax: 202–395–7285,
Email: OIRA_SUBMISSION@
OMB.EOP.GOV. Attn: Desk Officer for
the Administration for Children and
Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2013–22996 Filed 9–20–13; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: State Personal Responsibility
Education Program (PREP).
OMB No.: 0970–0380.
Description: The Patient Protection
and Affordable Care Act, 2010, also
known as health care reform, amended
Title V of the Social Security Act (42
U.S.C. 701 et seq.) as amended by
sections 2951 and 2952(c), by adding
section 513, authorizing the Personal
Responsibility Education Program
(PREP). The President signed into law
the Patient Protection and Affordable
Care Act on March 23, 2010, Public Law
111–148, which added the new PREP
formula grant program. The purpose of
this program is to educate adolescents
on both abstinence and contraception to
prevent pregnancy and sexually
transmitted infections (STIs); and at
least three adulthood preparation
subjects. The Personal Responsibility
Education grant program funding is
available for fiscal years 2010 through
2014. Pursuant to monitoring these state
programs, grantees submit a semiannual
report on their performance.
A request is being made to solicit
comments from the public on
paperwork reduction as it relates to
ACYF’s receipt of the following
document from applicants and
awardees:
Performance Progress Report
Respondents: 50 States and 9
Territories, to include, District of
Columbia, Puerto Rico, Virgin Islands,
Guam, American Samoa, Northern
Mariana Islands, the Federated States of
Micronesia, the Marshall Islands and
Palau
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden
hours per
response
Total
burden hours
Performance Progress Reports .......................................................................
59
2
16
1,888
Estimated Total Annual Burden
Hours: 1,888.
the Administration for Children and
Families.
Additional Information
Robert Sargis,
Reports Clearance Officer.
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,
Attn: ACF Reports Clearance Officer. All
requests should be identified by the title
of the information collection. Email
address: infocollection@acf.hhs.gov.
emcdonald on DSK67QTVN1PROD with NOTICES
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, Fax: 202–395–7285,
Email: OIRA_SUBMISSION@
OMB.EOP.GOV. Attn: Desk Officer for
VerDate Mar<15>2010
20:16 Sep 20, 2013
Jkt 229001
[FR Doc. 2013–22995 Filed 9–20–13; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0985]
Complex Issues in Developing Drug
and Biological Products for Rare
Diseases; Public Workshop; Request
for Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice of public workshop;
request for comments.
ACTION:
The Food and Drug Administration
(FDA) is announcing the following
public workshop entitled ‘‘Complex
Issues in Developing Drug and
Biological Products for Rare Diseases.’’
The purpose of the public workshop is
twofold: To discuss complex issues in
clinical trials for developing drug and
biological products (‘‘drugs’’) for rare
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
diseases, including endpoint
development and selection, use of
surrogate endpoints and the accelerated
approval pathway, clinical trial design,
conduct and analysis, safety
considerations, and dose selection; and
to discuss ways to encourage and
accelerate the development of new
therapies for pediatric rare diseases.
FDA is seeking input on these topics
from academic, clinical, and treating
communities; patients and advocacy
groups; industry; and governmental
agencies. Input from this public
workshop will help develop a strategic
plan to encourage and accelerate the
development of new therapies for rare
diseases.
Date and Time: The public workshop
will be held on January 6, 2014, from 8
a.m. to 5 p.m. and on January 7, 2014,
from 8 a.m. to 4:45 p.m.
Location: The public workshop will
be held at FDA’s White Oak Campus,
10903 New Hampshire Ave., Building
31 Conference Center, the Great Room
(Rm. 1503), Silver Spring, MD 20993–
0002. Entrance for the public meeting
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://
E:\FR\FM\23SEN1.SGM
23SEN1
]]>Agencies
[Federal Register Volume 78, Number 184 (Monday, September 23, 2013)]
[Notices]
[Page 58311]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-22995]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: State Personal Responsibility Education Program (PREP).
OMB No.: 0970-0380.
Description: The Patient Protection and Affordable Care Act, 2010,
also known as health care reform, amended Title V of the Social
Security Act (42 U.S.C. 701 et seq.) as amended by sections 2951 and
2952(c), by adding section 513, authorizing the Personal Responsibility
Education Program (PREP). The President signed into law the Patient
Protection and Affordable Care Act on March 23, 2010, Public Law 111-
148, which added the new PREP formula grant program. The purpose of
this program is to educate adolescents on both abstinence and
contraception to prevent pregnancy and sexually transmitted infections
(STIs); and at least three adulthood preparation subjects. The Personal
Responsibility Education grant program funding is available for fiscal
years 2010 through 2014. Pursuant to monitoring these state programs,
grantees submit a semiannual report on their performance.
A request is being made to solicit comments from the public on
paperwork reduction as it relates to ACYF's receipt of the following
document from applicants and awardees:
Performance Progress Report
Respondents: 50 States and 9 Territories, to include, District of
Columbia, Puerto Rico, Virgin Islands, Guam, American Samoa, Northern
Mariana Islands, the Federated States of Micronesia, the Marshall
Islands and Palau
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Performance Progress Reports................ 59 2 16 1,888
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 1,888.
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, Attn:
ACF 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, Fax: 202-395-7285,
Email: OIRA_SUBMISSION@OMB.EOP.GOV. Attn: Desk Officer for the
Administration for Children and Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2013-22995 Filed 9-20-13; 8:45 am]
BILLING CODE 4184-01-P
