Submission for OMB Review; Comment Request, 54342-54343 [2010-22132]
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54342
Federal Register / Vol. 75, No. 172 / Tuesday, September 7, 2010 / Notices
Bankshares of Fayetteville, Inc.,
Fayetteville, Arkansas, and thereby
indirectly acquire Bank of Fayetteville,
Fayetteville, Arkansas.
Board of Governors of the Federal Reserve
System, September 1, 2010.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. 2010–22156 Filed 9–3–10; 8:45 am]
BILLING CODE 6210–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection:
Comment Request
In compliance with the requirement
for opportunity for public comment on
proposed data collection projects
(section 3506(c)(2)(A) of Title 44, United
States Code, as amended by the
Paperwork Reduction Act of 1995, Pub.
L. 104–13), the Health Resources and
Services Administration (HRSA)
publishes periodic summaries of
proposed projects being developed for
submission to the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and draft instruments, e-mail
paperwork@hrsa.gov or call the HRSA
Reports Clearance Officer at (301) 443–
1129.
Comments are invited on: (a) The
proposed collection of information for
the proper performance of the functions
of the agency; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance 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.
Proposed Project: National Health
Service Corps Information Follow-up
Form—[New]
The National Health Service Corps
(NHSC) of the Bureau of Clinician
Recruitment and Service, HRSA, is
committed to improving the health of
the Nation’s underserved by uniting
communities in need with caring health
professionals and by supporting
communities’ efforts to build better
systems of care.
The NHSC Information Follow-up
Form, which NHSC will use when
Number of
respondents
Form
Responses
per
respondent
exhibiting at national and regional
conferences as well as when presenting
on campuses to health profession
students, is an optional form that a
health profession student, licensed
clinician, faculty member, or clinical
site administrator can fill out.
Individuals who submit the form to
NHSC, may ask questions and/or sign
up to receive periodic program updates
and other general information regarding
opportunities with the NHSC via e-mail.
An individual is free to discontinue
receiving communication from NHSC at
anytime by e-mailing
NHSCupdate@hrsa.gov. Completed
forms will contain information such as,
the names of the individuals, their
e-mail address(es), their city and State,
their phone number, the organization
where they are employed (or the school
which they attend), the year they intend
to graduate (if applicable), how they
heard about NHSC, which NHSC
programs they are interested in, etc.
Assistance in completing the form will
be given by the BCRS staff person (or
BCRS representative) who is present at
the event. Based on the FY10 exhibit
and presentation schedule, NHSC could
have gathered information from 2,400
individuals. Using this as a guide for
future years, the estimated annual
burden is as follows:
Total
responses
Hours per
response
Total
burden
hours
Information Follow-up Form ...........................................
2,400
1
2,400
.025 (90 seconds) .......
60
Total ........................................................................
2,400
1
2,400
.025 (90 seconds) .......
60
E-mail comments to
paperwork@hrsa.gov or mail the HRSA
Reports Clearance Officer, Room 10–33,
Parklawn Building, 5600 Fishers Lane,
Rockville, MD 20857. Written comments
should be received within 60 days of
this notice.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: September 1, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
Submission for OMB Review;
Comment Request
[FR Doc. 2010–22233 Filed 9–3–10; 8:45 am]
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BILLING CODE 4165–15–P
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Administration for Children and
Families
[OMB No.: 0970–0376]
Title: Strengthening Communities
Fund Program Evaluation.
Description: This proposed
information collection activity is to
obtain evaluation information from
Strengthening Communities Fund (SCF)
grantees. Grantees include participants
in two SCF grant programs contributing
to the economic recovery as authorized
in the American Recovery and
Reinvestment Act of 2009 (ARRA). The
SCF evaluation is an important
opportunity to examine the outcomes
achieved by the Strengthening
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Communities Fund in meeting its
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 is
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
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Federal Register / Vol. 75, No. 172 / Tuesday, September 7, 2010 / Notices
Nonprofit Capacity Building Program Performance Progress Report (PPR) ....................................................................................
Government Capacity Building Program PPR .................................
Estimated Total Annual Burden
Hours: 336.
Additional Information:
Copies of the proposed collection may
be obtained 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. All requests should be
identified by the title of the information
collection. E-mail 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,
E-mail:
OIRA_SUBMISSION@OMB.EOP.GOV.
Attn: Desk Officer for the
Administration for Children and
Families.
Dated: August 31, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–22132 Filed 9–3–10; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
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[Docket No. FDA–2010–N–0436]
Center for Biologics Evaluation and
Research eSubmitter Pilot Evaluation
Program for Blood Establishments
That Collect Whole Blood and Blood
Components
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA), Center for
Biologics Evaluation and Research
(CBER) is announcing an invitation to
participate in a pilot evaluation program
SUMMARY:
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Number of
responses per
respondent
Number of
respondents
Instrument
35
49
for CBER’s eSubmitter Program
(eSubmitter). CBER’s eSubmitter has
been customized as an automated
biologics license application (BLA) and
BLA supplement (BLS) submission
system for blood and blood components.
Participation in the pilot program is
open to blood establishments that
collect Whole Blood and blood
components. The pilot program is
intended to provide industry and CBER
regulatory review staff the opportunity
to evaluate the eSubmitter system and
determine if it facilitates the BLA/BLS
submission process. The purpose of this
notice is to invite blood establishments
that collect Whole Blood and blood
components to submit a request to CBER
if they are interested in participating in
this pilot program.
DATES: Submit a written or electronic
request for participation in this program
by October 7, 2010.
ADDRESSES: If you are interested in
participating in this program, you
should submit a request to participate in
the program to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Submit
electronic requests to https://
www.regulations.gov.
FOR FURTHER INFORMATION CONTACT: Lore
Fields, Center for Biologics Evaluation
and Research (HFM–375), Food and
Drug Administration, 1401 Rockville
Pike, suite 200N, Rockville, MD 20852–
1448, 301–827–6143, FAX: 301–827–
3534, email: lore.fields@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
CBER regulates certain biological
products, including blood and blood
products, and is committed to
advancing the public health through
innovative activities that help ensure
the safety, effectiveness and timely
delivery of these products to patients.
Further, CBER seeks to continuously
enhance and update review efficiency
and quality, and the quality of its
regulatory efforts and interactions, by
providing CBER staff and industry with
improved processes. In support of this
goal, CBER has participated in the FDA
development of a computer-assisted
automated BLA/BLS submission
program called eSubmitter to improve
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Average burden
hours per
response
4
4
Total burden
hours
1
1
140
196
the process for providing certain
regulatory submissions to FDA.
eSubmitter will include programs to
submit applications for licensure,
supplements to an approved license,
and amendments to pending
applications or supplements.
II. The eSubmitter Pilot Evaluation
Program Expectations
The eSubmitter pilot evaluation
program is expected to last
approximately 12 months. During this
period of time, participants will
complete BLA/BLS regulatory
submissions using the eSubmitter
template developed at CBER for use by
blood establishments that collect Whole
Blood and blood components.
eSubmitter was developed using the
same review criteria for applications for
these products as currently used in the
BLA/BLS review process at CBER.
During the BLA/BLS submission
process, the participants will enter the
requested information into the
eSubmitter tool and attach requested
documents as an Adobe document (pdf
format). This information will be saved
onto a CD–ROM and mailed to CBER for
review. Paper copies of submissions
will not be required. CBER will review
the information provided on the CD–
ROM and the attachments according to
current managed review procedures.
During the BLA/BLS submission
process, CBER staff will be available to
answer any questions or concerns that
may arise. As each submission is
completed, the users will be asked to
comment on the eSubmitter program.
These discussions will assist CBER in
the final development and release of
this electronic tool for use by industry.
III. Requests for Participation
Requests to participate in the
eSubmitter pilot are to be identified
with the docket number found in
brackets in the heading of this
document. You should include the
following information in your request:
Contact name, contact phone number,
email address, name of the
establishment, address, and license
number. Once requests for participation
are received, FDA will contact
interested establishments to discuss the
pilot program.
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Agencies
[Federal Register Volume 75, Number 172 (Tuesday, September 7, 2010)]
[Notices]
[Pages 54342-54343]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-22132]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
[OMB No.: 0970-0376]
Submission for OMB Review; Comment Request
Title: Strengthening Communities Fund Program Evaluation.
Description: This proposed information collection activity is to
obtain evaluation information from Strengthening Communities Fund (SCF)
grantees. Grantees include participants in two SCF grant programs
contributing to the economic recovery as authorized in the American
Recovery and Reinvestment Act of 2009 (ARRA). The SCF evaluation is an
important opportunity to examine the outcomes achieved by the
Strengthening Communities Fund in meeting its 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 is 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
[[Page 54343]]
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Nonprofit Capacity Building Program 35 4 1 140
Performance Progress Report (PPR)......
Government Capacity Building Program PPR 49 4 1 196
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 336.
Additional Information:
Copies of the proposed collection may be obtained 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. All requests
should be identified by the title of the information collection. E-mail
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, E-mail: OIRA_SUBMISSION@OMB.EOP.GOV. Attn: Desk Officer for the
Administration for Children and Families.
Dated: August 31, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010-22132 Filed 9-3-10; 8:45 am]
BILLING CODE 4184-01-P