Proposed Information Collection Activity; Comment Request, 19072-19073 [E8-7139]
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Federal Register / Vol. 73, No. 68 / Tuesday, April 8, 2008 / Notices
with project staff and marriage
education service providers in the
community will provide a detailed
understanding of the administration and
operation of the demonstrations. Focus
group discussions will provide insights
into participants’ perspectives on
marriage education and their
experiences with the CHMI
interventions.
In addition to the implementation
information collected under this
request, an impact evaluation will be
integrated with the implementation
study and will assess the effects of
healthy marriage initiatives by
comparing family and child well-being
outcomes in the CHMI communities
with similar outcomes in comparison
communities that are well-matched to
the project sites. Data from the
implementation studies will provide the
basis for the instrumental variable
models of CHMI impacts to help
determine direct or indirect exposure to
marriage-related services. Baseline data
collected under the impact evaluation
has been approved by OMB (i.e., Control
No. 0970–0322).
Respondents: Lead Project Staff;
Service Provider Organization Staff; Key
Community, Civic Stakeholders; and
Program Participants.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Average number of responses per
respondent
Average burden
hours per
response
Total burden
hours
Administrative Interviews ...............................................................................
Small Group Interviews .................................................................................
200
25
2
1
1
1.6
400
40
Estimated Total Annual Burden Hours ...................................................
........................
........................
..........................
440
pwalker on PROD1PC71 with NOTICES
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 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: OPREinfo
collection@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.
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Jkt 214001
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Dated: March 31, 2008.
Brendan C. Kelly,
OPRE Reports Clearance Officer.
[FR Doc. E8–7137 Filed 4–7–08; 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 Project
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
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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 inperson observations and site visits, in
order to integrate the perspectives of
program operators, policy officials and
members of the research community.
Following standard 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.
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08APN1
19073
Federal Register / Vol. 73, No. 68 / Tuesday, April 8, 2008 / Notices
ANNUAL BURDEN ESTIMATES
Number of
responses per
respondent
Number of
respondents
Instrument
Average
burden hours
per response
Total annual
burden hours
Semi-Structured Discussion and Information-Gathering Protocol ...................
600
1
.5
300
Estimated Total Annual Burden Hours .....................................................
........................
........................
........................
300
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 for Children and
Families, Office Planning, Research and
Evaluation, 370 L’Enfant Promenade,
SW., Washington, DC 20447, Attn: ACF
Reports Clearance Officer. E-mail
address:
OPREinfocollection@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: March 31, 2008.
Brendan C. Kelly,
OPRE Reports Clearance Officer.
[FR Doc. E8–7139 Filed 4–7–08; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
pwalker on PROD1PC71 with NOTICES
[Docket No. FDA–2008–N–0172]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; New Animal Drugs
for Investigational Use
AGENCY:
Food and Drug Administration,
HHS.
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16:09 Apr 07, 2008
Jkt 214001
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the reporting and recordkeeping
requirements for ‘‘New Animal Drugs
for Investigational Use.’’
DATES: Submit written or electronic
comments on the collection of
information by June 9, 2008.
ADDRESSES: Submit electronic
comments on the collection of
information to: https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of the Chief
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–827–
1472.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
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Sfmt 4703
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
New Animal Drugs for Investigational
Use—21 CFR Part 511 (OMB Control
Number 0910–0117)—Extension
FDA has authority under the Federal
Food, Drug, and Cosmetic Act (the act)
to approve new animal drugs. Section
512(j) of the act (21 U.S.C 360b(j)),
authorized FDA to issue regulations for
the investigational use of new animal
drugs. The regulations which set forth
conditions for investigational use of
new animal drugs are codified under
part 511 (21 CFR part 511). If a new
animal drug is only for tests in vitro, or
testing in laboratory research animals,
the person distributing the new animal
drug must maintain records showing: (1)
The name and post office address of the
expert or expert organization to whom
the drug is shipped; and (2) the date,
quantity, batch or code mark for each
shipment for a period of 2 years after
such shipment or delivery. Prior to
shipping a new animal drug for clinical
investigations in animals, a sponsor
must submit to FDA a Notice of Claimed
Investigational Exemption (NCIE). The
NCIE must contain, among other things,
the following specific information: (1)
The identity of the new animal drug; (2)
labeling; (3) a statement of compliance
E:\FR\FM\08APN1.SGM
08APN1
]]>Agencies
[Federal Register Volume 73, Number 68 (Tuesday, April 8, 2008)]
[Notices]
[Pages 19072-19073]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-7139]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Project
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 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.
[[Page 19073]]
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
----------------------------------------------------------------------------------------------------------------
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 for Children and Families, Office
Planning, Research and Evaluation, 370 L'Enfant Promenade, SW.,
Washington, DC 20447, Attn: ACF Reports Clearance Officer. E-mail
address: OPREinfocollection@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: March 31, 2008.
Brendan C. Kelly,
OPRE Reports Clearance Officer.
[FR Doc. E8-7139 Filed 4-7-08; 8:45 am]
BILLING CODE 4184-01-M
