Proposed Information Collection Activity; Comment Request, 19762 [05-7517]
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19762
Federal Register / Vol. 70, No. 71 / Thursday, April 14, 2005 / Notices
Place: Agency for Healthcare Research
& Quality, 540 Gaither Road, Conference
Center, Rockville, Maryland 20850.
Contact Person: Anyone wishing to
obtain information regarding this
meeting should contact Thomas Boyce,
Office of Performance Accountability,
Resources and Technology, Agency for
Healthcare Research and Quality, 540
Gaither Road, Rockville, Maryland
20850, (301) 427–1796.
Dated: April 4, 2005.
Carolyn M. Clancy,
Director.
[FR Doc. 05–7474 Filed 4–13–05; 8:45 am]
BILLING CODE 4160–90–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Compassion Capital Fund
Evaluation.
OMB No.: New Collection.
Description: This proposed
information collection activity is for two
rounds of surveys to be completed by
faith-based and community
organizations participating in the
Compassion Capital Fund (CCF)
evaluation project. The first survey will
be conducted as a baseline survey and
the second will be a follow-up survey
conducted several months later.
The CCF evaluation is an important
opportunity to examine the
effectiveness of the Compassion Capital
Fund in meeting its objective of
improving the capacity of faith-based
and community organizations. The
evaluation will involve up to 1,000
faith-based and community
organizations that seek services from
CCF-funded intermediary organizations.
Information will be collected from these
faith-based and community-based
organizations to assess change and
improvement in various areas of
capacity. The study design includes the
random assignment of faith-based and
community organizations to either a
treatment group that receives capacitybuilding services from a CCF
intermediary grantee or to a control
group that does not. The impact of the
Number of
respondents
Instrument
services provided by intermediaries,
primarily through sub-awards and/or
technical assistance (TA), will be
determined by comparing the changes
in organizational and service capacity of
the recipient organizations with those of
the control group.
Respondents: The respondents for
both the baseline and follow-up data
collection will be faith-based and
community organizations that seek subawards or TA from selected CCF
intermediary grantees. The baseline
survey will be primarily selfadministered and is expected to be
completed as part of the intermediary’s
sub-award application or TA request
process. The follow-up survey also will
be primarily self-administered and
contain questions similar to those in the
baseline survey as well as additional
questions related to services received
from the intermediary or other
organizations. It is expected that the
follow-up survey will be administered
approximately 9–12 months after
random assignment. As needed to
increase response rates, the survey will
be administered by telephone to
organizations that do not initially return
a completed survey.
Number of responses per respondent
Average burden hours per response
Total
burden
hours
Baseline Survey ....................................................
Follow-up Survey ..................................................
1,000
1,000
............................
............................
1.33 hours (20 minutes) .......................................
1.42 hours (25 minutes) .......................................
330
420
Estimated Total Annual Burden Hours ..........
....................
............................
..........................................................................
750
Annual Burden Estimates
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 Administration,
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447. Attn: ACF Reports Clearance
Officer. E-mail address:
grjohnson@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
VerDate jul<14>2003
19:36 Apr 13, 2005
Jkt 205001
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. Consideration will be
given to comments and suggestions
submitted within 60 days of this
publication.
Dated: April 11, 2005.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 05–7517 Filed 4–13–05; 8:45 am]
BILLING CODE 4184–01–M
PO 00000
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 1979N–0113 (formerly Docket
No. 79N–0113); DESI 2847]
Drugs for Human Use; Drug Efficacy
Study Implementation; Parenteral
Multivitamin Drug Products;
Announcement of Unlawful
Formulations
Food and Drug Administration.
Notice.
AGENCY:
ACTION:
SUMMARY: The Food and Drug
Administration (FDA) is declaring
unlawful the unapproved marketing of
certain parenteral multivitamin drug
products for which a hearing was
requested, but for which the sponsors
have withdrawn the hearing requests.
FDA is taking this action because the
products lack substantial evidence of
effectiveness as fixed combination drug
products.
E:\FR\FM\14APN1.SGM
14APN1
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[Federal Register Volume 70, Number 71 (Thursday, April 14, 2005)]
[Notices]
[Page 19762]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-7517]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: Compassion Capital Fund Evaluation.
OMB No.: New Collection.
Description: This proposed information collection activity is for
two rounds of surveys to be completed by faith-based and community
organizations participating in the Compassion Capital Fund (CCF)
evaluation project. The first survey will be conducted as a baseline
survey and the second will be a follow-up survey conducted several
months later.
The CCF evaluation is an important opportunity to examine the
effectiveness of the Compassion Capital Fund in meeting its objective
of improving the capacity of faith-based and community organizations.
The evaluation will involve up to 1,000 faith-based and community
organizations that seek services from CCF-funded intermediary
organizations. Information will be collected from these faith-based and
community-based organizations to assess change and improvement in
various areas of capacity. The study design includes the random
assignment of faith-based and community organizations to either a
treatment group that receives capacity-building services from a CCF
intermediary grantee or to a control group that does not. The impact of
the services provided by intermediaries, primarily through sub-awards
and/or technical assistance (TA), will be determined by comparing the
changes in organizational and service capacity of the recipient
organizations with those of the control group.
Respondents: The respondents for both the baseline and follow-up
data collection will be faith-based and community organizations that
seek sub-awards or TA from selected CCF intermediary grantees. The
baseline survey will be primarily self-administered and is expected to
be completed as part of the intermediary's sub-award application or TA
request process. The follow-up survey also will be primarily self-
administered and contain questions similar to those in the baseline
survey as well as additional questions related to services received
from the intermediary or other organizations. It is expected that the
follow-up survey will be administered approximately 9-12 months after
random assignment. As needed to increase response rates, the survey
will be administered by telephone to organizations that do not
initially return a completed survey.
----------------------------------------------------------------------------------------------------------------
Number of Total
Instrument Number of responses per Average burden hours per burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Baseline Survey........................... 1,000 ................ 1.33 hours (20 minutes)..... 330
Follow-up Survey.......................... 1,000 ................ 1.42 hours (25 minutes)..... 420
--------
Estimated Total Annual Burden Hours... ........... ................ ............................ 750
----------------------------------------------------------------------------------------------------------------
Annual Burden Estimates
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
Administration, Office of Information Services, 370 L'Enfant Promenade,
SW., Washington, DC 20447. Attn: ACF Reports Clearance Officer. E-mail
address: grjohnson@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. Consideration will be given to comments
and suggestions submitted within 60 days of this publication.
Dated: April 11, 2005.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 05-7517 Filed 4-13-05; 8:45 am]
BILLING CODE 4184-01-M