Submission for OMB Review; Comment Request, 44272 [E8-17353]
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44272
Federal Register / Vol. 73, No. 147 / Wednesday, July 30, 2008 / Notices
Dated: July 16, 2008.
Brendan C. Kelly,
OPRE Reports Clearance Officer.
[FR Doc. E8–17352 Filed 7–29–08; 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
Proposed Projects
Title: Generic Clearance To Conduct
Qualitative Data Collections.
OMB No.: New Collection.
Description: The Office of Planning,
Research and Evaluation (OPRE),
Administration for Children and
Families (ACF), U.S. Department of
Health and Human Services (HHS),
intends to request approval from the
Office of Management and Budget
(OMB) for a generic clearance that will
allow OPRE to conduct a variety of
qualitative data collections. Over the
next three years, OPRE anticipates
undertaking a variety of new research
projects in the fields of cash welfare,
employment and self-sufficiency, Head
Start, child care, healthy marriage and
responsible fatherhood, and child
welfare. In order to inform the
development of OPRE research, to
maintain a research agenda that is
rigorous and relevant, and to ensure that
research products are as current as
possible, OPRE will engage in a variety
of qualitative data collections in concert
with researchers and practitioners
throughout the field. OPRE envisions
using a variety of techniques including
semi-structured discussions, focus
groups, telephone interviews, and in
person observations and site visits, in
order to integrate the perspectives of
program operators, policy officials and
members of the research community.
Following standard Office of
Management and Budget (OMB)
requirements, OPRE will submit a
change request to OMB individually for
every group of data collection activities
undertaken under this generic
clearance. OPRE will provide OMB with
a copy of the individual instruments or
questionnaires (if one is used), as well
as other materials describing the project.
Respondents: Administrators or staff
of State and local agencies or programs
in the relevant fields; academic
researchers; and policymakers at various
levels of government.
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average burden hours per
response
Total annual
burden hours
Semi-Structured Discussion and Information-Gathering Protocol ...................
600
1
.5
300
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Estimated Total Annual Burden
Hours: 300.
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. E-mail address:
OPRElnfoCollection@acf.hhs.gov. All
requests should be identified by the title
of the information collection.
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.
Dated: July 16, 2008.
Brendan C. Kelly,
OPRE Reports Clearance Officer.
[FR Doc. E8–17353 Filed 7–29–08; 8:45 am]
BILLING CODE 4184–01–M
VerDate Aug<31>2005
23:06 Jul 29, 2008
Jkt 214001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–D–0379]
Draft Guidance for Industry: Nucleic
Acid Testing to Reduce the Possible
Risk of Parvovirus B19 Transmission
by Plasma-Derived Products;
Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of a draft document entitled
‘‘Guidance for Industry: Nucleic Acid
Testing (NAT) to Reduce the Possible
Risk of Parvovirus B19 Transmission by
Plasma-Derived Products,’’ dated July
2008. The draft guidance document
provides to manufacturers of plasmaderived products recommendations for
performing parvovirus B19 NAT as an
in-process test for Source Plasma and
recovered plasma to identify and help to
prevent the use of plasma units
containing high levels of parvovirus
B19. The draft guidance also
recommends how to report to the FDA
implementation of parvovirus B19 NAT.
DATES: Although you can comment on
any guidance at any time (see 21 CFR
10.115 (g)(5)), to ensure that the agency
PO 00000
Frm 00062
Fmt 4703
Sfmt 4703
considers your comment on this draft
guidance before it begins work on the
final version of the guidance, submit
written or electronic comments on the
draft guidance by October 28, 2008.
Submit written requests for
single copies of the draft guidance to the
Office of Communication, Training, and
Manufacturers Assistance (HFM–40),
Center for Biologics Evaluation and
Research (CBER), Food and Drug
Administration, 1401 Rockville Pike,
suite 200N, Rockville, MD 20852–1448.
Send one self-addressed adhesive label
to assist the office in processing your
requests. The draft guidance may also be
obtained by mail by calling CBER at 1–
800–835–4709 or 301–827–1800. See
the SUPPLEMENTARY INFORMATION section
for electronic access to the draft
guidance document.
Submit written comments on the draft
guidance to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Submit
electronic comments to https://
www.regulations.gov.
ADDRESSES:
Paul
E. Levine, Jr., Center for Biologics
Evaluation and Research (HFM–17),
Food and Drug Administration, 1401
Rockville Pike, suite 200N, Rockville,
MD 20852–1448, 301–827–6210.
FOR FURTHER INFORMATION CONTACT:
SUPPLEMENTARY INFORMATION:
E:\FR\FM\30JYN1.SGM
30JYN1
]]>Agencies
[Federal Register Volume 73, Number 147 (Wednesday, July 30, 2008)]
[Notices]
[Page 44272]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-17353]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Proposed Projects
Title: Generic Clearance To Conduct Qualitative Data Collections.
OMB No.: New Collection.
Description: The Office of Planning, Research and Evaluation
(OPRE), Administration for Children and Families (ACF), U.S. Department
of Health and Human Services (HHS), intends to request approval from
the Office of Management and Budget (OMB) for a generic clearance that
will allow OPRE to conduct a variety of qualitative data collections.
Over the next three years, OPRE anticipates undertaking a variety of
new research projects in the fields of cash welfare, employment and
self-sufficiency, Head Start, child care, healthy marriage and
responsible fatherhood, and child welfare. In order to inform the
development of OPRE research, to maintain a research agenda that is
rigorous and relevant, and to ensure that research products are as
current as possible, OPRE will engage in a variety of qualitative data
collections in concert with researchers and practitioners throughout
the field. OPRE envisions using a variety of techniques including semi-
structured discussions, focus groups, telephone interviews, and in
person observations and site visits, in order to integrate the
perspectives of program operators, policy officials and members of the
research community.
Following standard Office of Management and Budget (OMB)
requirements, OPRE will submit a change request to OMB individually for
every group of data collection activities undertaken under this generic
clearance. OPRE will provide OMB with a copy of the individual
instruments or questionnaires (if one is used), as well as other
materials describing the project.
Respondents: Administrators or staff of State and local agencies or
programs in the relevant fields; academic researchers; and policymakers
at various levels of government.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total annual
respondents respondent response burden hours
----------------------------------------------------------------------------------------------------------------
Semi-Structured Discussion and Information- 600 1 .5 300
Gathering Protocol.........................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 300.
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. E-mail
address: OPRElnfoCollection@acf.hhs.gov. All requests should be
identified by the title of the information collection.
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.
Dated: July 16, 2008.
Brendan C. Kelly,
OPRE Reports Clearance Officer.
[FR Doc. E8-17353 Filed 7-29-08; 8:45 am]
BILLING CODE 4184-01-M
