Submission for OMB Review; Comment Request, 4712-4713 [07-431]
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4712
Federal Register / Vol. 72, No. 21 / Thursday, February 1, 2007 / Notices
Description: The Annual Survey of
Refugees collects information on the
social and economic circumstances of a
random sample of refugees, Amerasians,
and entrants who arrived in the United
States in the five years prior to the date
of the survey. The survey focuses on the
refugees’ training, labor force
participation, and welfare utilization
rates. Data are segmented by region of
origin, State of resettlement, and
number of months since arrival. From
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects:
Title: Annual Survey of Refugees.
OMB No.: 0970–0033.
the responses, the Office of Refugee
Resettlement reports on the economic
adjustment of refugees to the American
economy. These data are used by
Congress in its annual deliberations of
refugee admissions and funding and by
program managers in formulating
policies for the future direction of the
Refugee Resettlement Program.
Respondents: Refugees, entrants,
Amerasians, and Havana parolees.
Annual Burden Estimates:
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
ORR–9 .............................................................................................................
2,000
1
.666666
1,333
Estimated Total Annual Burden
Hours: 1,333.
In compliance with the requirements
of Section 3506(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 of 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.
Dated: January 25, 2007.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 07–430 Filed 1–31–07; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Compassion Capital Fund
Evaluation—Indicators of
Organizational Capacity Among
Targeted Capacity Building Program
Grantees.
OMB No.: New Collection.
Description: This information
collection activity is for a study of
grantees under the Targeted Capacity
Building Program that is one component
of the evaluation of the Compassion
Capital Fund (CCF) program. The
information collection will be through
mailed surveys to be completed by
selected faith-based and community
organizations that received Targeted
Capacity Building grants under the CCF
program.
The overall evaluation includes
multiple components that will examine
indicators, outcomes and effectiveness
of the CCF in meeting its objective of
improving the capacity of faith-based
and community organizations. This
component of the evaluation will
involve approximately 309 faith-based
and community organizations.
Information will be sought from these
organizations to assess change and
improvement in various areas of
organizational capacity resulting from
receipt of a Targeted Capacity Building
grant.
Respondents: The respondents will be
selected faith-based and community
organizations that received a Targeted
Capacity Building grant in a prior year.
The surveys will be self-administered.
Annual Burden Estimates:
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Indicators of Organizational Capacity Survey .................................................
rwilkins on PROD1PC63 with NOTICES
Instrument
309
1
.499
154
Estimated Total Annual Burden
Hours: 154.
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
VerDate Aug<31>2005
16:47 Jan 31, 2007
Jkt 211001
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.
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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: 202–395–6974.
Attn: Desk Officer for ACF.
E:\FR\FM\01FEN1.SGM
01FEN1
Federal Register / Vol. 72, No. 21 / Thursday, February 1, 2007 / Notices
Dated: January 25, 2007.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 07–431 Filed 1–31–07; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4184–01–M
[Docket No. 2004N–0408]
Food and Drug Administration
Regulatory Site Visit Training Program
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
AGENCY:
Food and Drug Administration,
HHS.
Food and Drug Administration
ACTION:
[Docket No. 2006N–0239]
SUMMARY: The Food and Drug
Administration’s (FDA’s) Center for
Biologics Evaluation and Research
(CBER) is reannouncing the invitation
for participation in its Regulatory Site
Visit Training Program (RSVP). This
training program is intended to give
CBER regulatory review, compliance,
and other relevant staff an opportunity
to visit biologics facilities. These visits
are intended to allow CBER staff to
directly observe routine manufacturing
practices and to give CBER staff a better
understanding of the biologics industry,
including its challenges and operations.
The purpose of this notice is to invite
biologics facilities to contact CBER for
more information if they are interested
in participating in this program.
DATES: Submit written or electronic
requests for participation in this
program by March 5, 2007. The request
should include a description of your
facility relative to products regulated by
CBER. Please specify the physical
address of the site you are offering.
ADDRESSES: If your biologics facility is
interested in offering a site visit or
learning more about this training
opportunity for CBER staff, 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.fda.gov/dockets/ecomments.
If your biologics facility responded to
the previous RSVP notice announced in
the Federal Register of April 11, 2006
(71 FR 18340), and your facility wishes
to continue to be considered for this
year’s program, please notify CBER of
your continued interest by sending an email to matt@cber.fda.gov.
FOR FURTHER INFORMATION CONTACT:
Lonnie Warren-Myers, Division of
Manufacturers Assistance and Training,
Center for Biologics Evaluation and
Research (HFM–49), Food and Drug
Administration, 1401 Rockville Pike,
suite 200N, Rockville, MD 20852–1448,
301–827–2000, FAX: 301–827–3079, email: matt@cber.fda.gov.
SUPPLEMENTARY INFORMATION:
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Infectious Disease in
Xenotransplantation
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Infectious Disease in
Xenotransplantation’’ has been
approved by the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT:
Jonna Capezzuto, Office of the Chief
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–827–
4659.
In the
Federal Register of October 31, 2006 (71
FR 63768), the agency announced that
the proposed information collection had
been submitted to OMB for review and
clearance under 44 U.S.C. 3507. An
agency may not conduct or sponsor, and
a person is not required to respond to,
a collection of information unless it
displays a currently valid OMB control
number. OMB has now approved the
information collection and has assigned
OMB control number 0910–0456. The
approval expires on January 31, 2010. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.fda.gov/
ohrms/dockets.
rwilkins on PROD1PC63 with NOTICES
SUPPLEMENTARY INFORMATION:
Dated: January 25, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–1550 Filed 1–31–07; 8:45 am]
BILLING CODE 4160–01–S
VerDate Aug<31>2005
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Notice.
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4713
I. Background
CBER regulates certain biological
products including blood and blood
products, vaccines, and cellular, tissue
and gene therapies. CBER is committed
to advancing the public health through
innovative activities that help ensure
the safety, effectiveness, and timely
delivery of biological products to
patients. To support this primary goal,
CBER has initiated various training and
development programs to promote high
performance of its compliance staff,
regulatory review staff, and other
relevant staff. CBER seeks to
continuously enhance and update
review efficiency and quality, and the
quality of its regulatory efforts and
interactions, by providing CBER staff
with a better understanding of the
biologics industry and its operations.
Further, CBER seeks to improve: (1) Its
understanding of current industry
practices, and regulatory impacts and
needs; and (2) communication between
CBER staff and industry. CBER initiated
its RSVP in 2005, and through these
annual notices, is requesting those firms
that have previously applied and are
still interested in participating, to
reaffirm their interest, as well as
encouraging new interested parties to
apply.
II. RSVP
A. Regulatory Site Visits
In this program, over a period of time
to be agreed upon with the facility,
small groups of CBER staff may observe
operations of biologics establishments,
including, for example, blood and tissue
establishments. The visits may include
packaging facilities, quality control and
pathology/toxicology laboratories, and
regulatory affairs operations. These
visits, or any part of the program, are
not intended as a mechanism to inspect,
assess, judge, or perform a regulatory
function, but are meant to improve
mutual understanding and to provide an
avenue for open dialogue between the
biologics industry and CBER.
B. Site Selection
All travel expenses associated with
the site visits will be the responsibility
of CBER; therefore, selection of potential
facilities will be based on the
coordination of CBER’s priorities for
staff training as well as the limited
available resources for this program. In
addition to logistical and other resource
factors to consider, a key element of site
selection is a successful compliance
record with CBER or another agency for
which we have a memorandum of
understanding.
E:\FR\FM\01FEN1.SGM
01FEN1
Agencies
[Federal Register Volume 72, Number 21 (Thursday, February 1, 2007)]
[Notices]
[Pages 4712-4713]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 07-431]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Compassion Capital Fund Evaluation--Indicators of
Organizational Capacity Among Targeted Capacity Building Program
Grantees.
OMB No.: New Collection.
Description: This information collection activity is for a study of
grantees under the Targeted Capacity Building Program that is one
component of the evaluation of the Compassion Capital Fund (CCF)
program. The information collection will be through mailed surveys to
be completed by selected faith-based and community organizations that
received Targeted Capacity Building grants under the CCF program.
The overall evaluation includes multiple components that will
examine indicators, outcomes and effectiveness of the CCF in meeting
its objective of improving the capacity of faith-based and community
organizations. This component of the evaluation will involve
approximately 309 faith-based and community organizations. Information
will be sought from these organizations to assess change and
improvement in various areas of organizational capacity resulting from
receipt of a Targeted Capacity Building grant.
Respondents: The respondents will be selected faith-based and
community organizations that received a Targeted Capacity Building
grant in a prior year. The surveys will be self-administered.
Annual Burden Estimates:
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Indicators of Organizational Capacity Survey 309 1 .499 154
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 154.
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-
6974. Attn: Desk Officer for ACF.
[[Page 4713]]
Dated: January 25, 2007.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 07-431 Filed 1-31-07; 8:45 am]
BILLING CODE 4184-01-M