Proposed Information Collection Activity; Comment Request, 18847-18848 [2010-8426]
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18847
Federal Register / Vol. 75, No. 70 / Tuesday, April 13, 2010 / Notices
objective of improving the capacity of
grantees that include Nonprofit
organizations and State, Local and
Tribal Governments. The evaluation for
each program will be designed to assess
progress and measure increased
organizational capacity of grantees in
each of the two SCF programs. The
purpose of this request will be to
establish the approved baseline
instruments for follow-up data
collection.
Respondents: SCF Grantees (both the
Nonprofit Capacity Building Program
and the Government Capacity Building
Program) made up of State, local, and
Tribal governments, as well as nonprofit
organizations.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Nonprofit Capacity Building Program Performance Progress Report (PPR) ..
Government Capacity Building PPR ................................................................
Average burden hours per
response
4
4
1
1
35
49
Estimated Total Annual Burden
Hours: 336.
Washington, DC 20503, FAX (202) 395–
6974.
Additional Information
Robert Sargis,
Reports Clearance Officer.
ACF is requesting that OMB grant a
180 day approval for this information
collection under procedures for
emergency processing by April 15, 2010.
A copy of this information collection,
with applicable supporting
documentation, may be obtained by
calling the Administration for Children
and Families, Reports Clearance Officer,
Robert Sargis at (202) 690–7275.
Comments and questions about the
information collection described above
should be directed to the Office of
Information and Regulatory Affairs,
Attn: OMB Desk Officer for ACF, Office
of Management and Budget, Paperwork
Reduction Project, 725 17th Street, NW.,
Number of responses per
respondent
[FR Doc. 2010–8251 Filed 4–12–10; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: ADP & Services Conditions for
FFP for ACF.
OMB No.: 0992–0005.
Description: The Advance Planning
Document (APD) process, established in
the rules at 45 CFR part 95, subpart F,
Total burden
hours
140
196
is the procedure by which States request
and obtain approval for Federal
financial participation in their cost of
acquiring Automatic Data Processing
(ADP) equipment and services. State
agencies that submit APD requests
provide the Department of Health and
Human Services (HHS) with the
following information necessary to
determine the States’ needs to acquire
the requested ADP equipment and/or
services:
(1) A statement of need;
(2) A requirements analysis and
feasibility study;
(3) A cost benefit analysis;
(4) A proposed activity schedule; and,
(5) A proposed budget.
HHS’ determination of a State
Agency’s need to acquire requested ADP
equipment or services is authorized at
sections 402(a)(5), 452(a)(1), 1902(a)(4),
and 1102 of the Social Security Act.
Respondents: States.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
sroberts on DSKD5P82C1PROD with NOTICES
Advance Planning Document ..........................................................................
RFP and Contract ............................................................................................
Emergency Funding Request ..........................................................................
Service Agreements ........................................................................................
Biennial Reports ..............................................................................................
Estimated Total Annual Burden
Hours: 5,751.50
In compliance with the requirements
of section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families 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 the Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
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17:33 Apr 12, 2010
Jkt 220001
Frm 00065
Fmt 4703
Sfmt 4703
Average burden hours per
response
1.84
1.54
1
1
1
60
1.50
1
1
1.50
50
50
27
14
50
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. E-mail address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions 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)
PO 00000
Number of responses per
respondent
Total burden
hours
5,520
115.50
27
14
75
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
E:\FR\FM\13APN1.SGM
13APN1
18848
Federal Register / Vol. 75, No. 70 / Tuesday, April 13, 2010 / Notices
Dated: April 8, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–8426 Filed 4–12–10; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0001]
Preparation for International
Conference on Harmonisation Steering
Committee and Expert Working Group
Meetings in Tallinn, Estonia; Regional
Public Meeting
AGENCY:
Food and Drug Administration,
HHS.
sroberts on DSKD5P82C1PROD with NOTICES
ACTION:
Notice of meeting.
SUMMARY: The Food and Drug
Administration (FDA) is announcing a
public meeting entitled ‘‘Preparation for
ICH Steering Committee and Expert
Working Group Meetings in Tallinn,
Estonia’’ to provide information and
receive comments on the International
Conference on Harmonisation (ICH) as
well as the upcoming meetings in
Tallinn, Estonia. The topics to be
discussed are the topics for discussion
at the forthcoming ICH Steering
Committee Meeting. The purpose of the
meeting is to solicit public input prior
to the next Steering Committee and
Expert Working Group meetings in
Tallinn, Estonia, June 5 through 10,
2010, at which discussion of the topics
underway and the future of ICH will
continue.
Date and Time: The meeting will be
held on Wednesday, May 5, 2010, from
2:30 p.m. to 4:30 p.m.
Location: The meeting will be held at
the Washington Theater at the Hilton
Washington DC/Rockville Hotel &
Executive Meeting Center, 1750
Rockville Pike, Rockville, MD 20852.
Contact Person: All participants must
register with Jennifer Haggerty, Office of
the Commissioner, Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, by e-mail:
jennifer.haggerty@fda.hhs.gov or FAX:
301–827–0003.
Registration and Requests for Oral
Presentations: Send registration
information (including name, title, firm
name, address, telephone, and fax
number), written material and requests
to make oral presentations, to the
contact person by April 30, 2010.
Interested persons may present data,
information, or views orally or in
writing, on issues pending at the public
meeting. Public oral presentations will
VerDate Nov<24>2008
17:33 Apr 12, 2010
Jkt 220001
be scheduled between approximately 4
p.m. and 4:30 p.m. Time allotted for oral
presentations may be limited to 10
minutes. Those desiring to make oral
presentations should notify the contact
person by April 30, 2010, and submit a
brief statement of the general nature of
the evidence or arguments they wish to
present, the names and addresses,
phone number, fax, and e-mail of
proposed participants, and an
indication of the approximate time
requested to make their presentation.
The agenda for the public meeting
will be made available via the Internet
at: https://www.fda.gov/Drugs/
NewsEvents/ucm204924.htm.
If you need special accommodations
due to a disability, please contact
Jennifer Haggerty at least 7 days in
advance.
Transcripts: Please be advised that as
soon as a transcript is available, it can
be obtained in either hardcopy or on
CD–ROM, after submission of a
Freedom of Information request. Written
requests are to be sent to Division of
Freedom of Information (HFI–35), Office
of Management Programs, Food and
Drug Administration, 5600 Fishers
Lane, rm. 6–30, Rockville, MD 20857.
SUPPLEMENTARY INFORMATION: The ICH
was established in 1990 as a joint
regulatory/industry project to improve,
through harmonization, the efficiency of
the process for developing and
registering new medicinal products in
Europe, Japan, and the United States
without compromising the regulatory
obligations of safety and effectiveness.
In recent years, many important
initiatives have been undertaken by
regulatory authorities and industry
associations to promote international
harmonization of regulatory
requirements. FDA has participated in
many meetings designed to enhance
harmonization and is committed to
seeking scientifically based harmonized
technical procedures for pharmaceutical
development. One of the goals of
harmonization is to identify and then
reduce differences in technical
requirements for medical product
development among regulatory
agencies. ICH was organized to provide
an opportunity for harmonization
initiatives to be developed with input
from both regulatory and industry
representatives. ICH is concerned with
harmonization among three regions: The
European Union, Japan, and the United
States. The six ICH sponsors are the
European Commission; the European
Federation of Pharmaceutical Industries
Associations; the Japanese Ministry of
Health, Labor and Welfare; the Japanese
Pharmaceutical Manufactures
PO 00000
Frm 00066
Fmt 4703
Sfmt 4703
Association; the Centers for Drug
Evaluation and Research and Biologics
Evaluation and Research, FDA; and the
Pharmaceutical Research and
Manufacturers of America. The ICH
Secretariat, which coordinates the
preparation of documentation, is
provided by the International
Federation of Pharmaceutical
Manufacturers Associations (IFPMA).
The ICH Steering Committee includes
representatives from each of the ICH
sponsors and Health Canada, the
European Free Trade Area, and the
World Health Organization. The ICH
process has achieved significant
harmonization of the technical
requirements for the approval of
pharmaceuticals for human use in the
three ICH regions.
The current ICH process and structure
can be found at the following Web site:
https://www.ich.org.
Dated: April 5, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–8379 Filed 4–12–10; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Prevention
Research Centers Comparative
Effectiveness Research Program, DP
10–003, Initial Review
In accordance with Section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the aforementioned meeting:
Times and Dates: 8:30 a.m.–6 p.m., May 4,
2010 (Closed); 8:30 a.m.–5 p.m., May 5, 2010
(Closed).
Place: W Hotel, 1111 Perimeter Center W.,
Atlanta, GA 30346.
Telephone: (770) 396–6800.
Status: The meeting will be closed to the
public in accordance with provisions set
forth in Section 552b(c)(4) and (6), Title 5
U.S.C., and the Determination of the Director,
Management Analysis and Services Office,
CDC, pursuant to Public Law 92–463.
Matters To Be Discussed: The meeting will
include the initial review, discussion, and
evaluation of applications received in
response to ‘‘Prevention Research Centers
Comparative Effectiveness Research Program,
DP 10–003.’’
Contact Person for More Information:
Donald Blackman, PhD, Scientific Review
Officer, National Center for Chronic Disease
Prevention and Health Promotion, Office of
the Director, Extramural Research Program
E:\FR\FM\13APN1.SGM
13APN1
]]>Agencies
[Federal Register Volume 75, Number 70 (Tuesday, April 13, 2010)]
[Notices]
[Pages 18847-18848]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-8426]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: ADP & Services Conditions for FFP for ACF.
OMB No.: 0992-0005.
Description: The Advance Planning Document (APD) process,
established in the rules at 45 CFR part 95, subpart F, is the procedure
by which States request and obtain approval for Federal financial
participation in their cost of acquiring Automatic Data Processing
(ADP) equipment and services. State agencies that submit APD requests
provide the Department of Health and Human Services (HHS) with the
following information necessary to determine the States' needs to
acquire the requested ADP equipment and/or services:
(1) A statement of need;
(2) A requirements analysis and feasibility study;
(3) A cost benefit analysis;
(4) A proposed activity schedule; and,
(5) A proposed budget.
HHS' determination of a State Agency's need to acquire requested
ADP equipment or services is authorized at sections 402(a)(5),
452(a)(1), 1902(a)(4), and 1102 of the Social Security Act.
Respondents: States.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Advance Planning Document....................... 50 1.84 60 5,520
RFP and Contract................................ 50 1.54 1.50 115.50
Emergency Funding Request....................... 27 1 1 27
Service Agreements.............................. 14 1 1 14
Biennial Reports................................ 50 1 1.50 75
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 5,751.50
In compliance with the requirements of section 506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families 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 the Administration for Children and Families, Office of
Administration, Office of Information Services, 370 L'Enfant Promenade,
SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. E-mail
address: infocollection@acf.hhs.gov. All requests should be identified
by the title of the information collection.
The Department specifically requests comments on: (a) Whether the
proposed collection of information is necessary for the proper
performance of the functions 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; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
[[Page 18848]]
Dated: April 8, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010-8426 Filed 4-12-10; 8:45 am]
BILLING CODE 4184-01-P
