Proposed Information Collection Activity; Comment Request, 30141-30142 [06-4851]
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Federal Register / Vol. 71, No. 101 / Thursday, May 25, 2006 / Notices
III. Eligibility Criteria and Other
Requirements
1. Eligible Applicants
Only states that received an AoA and
CMS Aging and Disability Resource
Center Grant in FY 2003 are eligible to
apply. These states are Louisiana,
Maine, Maryland, Massachusetts,
Minnesota, Montana, New Hampshire,
New Jersey, Pennsylvania, Rhode
Island, South Carolina, and West
Virginia.
Only the state agency that was the
ADRC applicant in FY 2003, or a state
agency with a Memorandum of
Agreement with the existing ADRC
grantee (e.g. the Single State Agency on
Aging, Single State Medicaid Agency or
State Agency serving the target
populations of people with disabilities)
may apply for this Resource Center
grant. The applicant agency must have
the documented support, in the form of
a Memorandum of Understanding and
active participation by the Single State
Agency on Aging, the Single State
Medicaid Agency and the State
Agency(s) serving the target
population(s) of people with disabilities
specified in the applicant’s proposal.
A letter of support from the Governor
indicating high-level state executive
support and designating the lead agency
is also required. Only one application
per state will be accepted. ‘‘State’’ refers
to the definition provided under 45 CFR
74.2. Executive Order 12372 is not
applicable to these grant applications.
2. Cost Sharing or Matching
Grantees are required to make a nonfinancial or cash recipient contribution
(match) of a minimum of five percent
(5%) of the total grant award.
3. DUNS Number
All grant applicants must obtain a D–
U–N–S number from Dun and
Bradstreet. It is a nine-digit
identification number, which provides
unique identifiers of single business
entities. The D–U–N–S number is free
and easy to obtain from https://
www.dnb.com/US/duns_update/.
4. Intergovernmental Review
Executive Order 12372,
Intergovernmental Review of Federal
Programs, is not applicable to these
grant applications.
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IV. Application and Submission
Information
1. Address To Request Application
Package
Application materials can be obtained
from https://www.grants.gov or https://
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www.aoa.gov/doingbus/fundopp/
fundopp.asp. Application materials are
also available by writing to: U.S.
Department of Health and Human
Services, Administration on Aging, John
Murphy, Center for Planning and Policy
Development, Washington, DC 20201.
Or by calling: 202–357–0136. Or emailing: john.murphy@aoa.hhs.gov.
2. Address for Application Submission
Electronic submissions must be sent
to: https://www.grants.gov.
Applicants unable to submit their
application via www.grants.gov may
request permission to submit a hard
copy from the AoA Project Officer: Greg
Case: greg.case@aoa.hhs.gov. (202) 357–
3442.
If you mail or hand delivers your
application, you must submit one
original application and two copies,
plus a completed application checklist
to AoA. The application deadline for
applications sent by U.S. Postal Service
must be post-marked by midnight July
21, 2006 or hand-delivered by 5 p.m.
Eastern Time on July 21, 2006.
Submissions using the regular, U.S.
Postal Service must be addressed
to:Department of Health and Human
Services, Administration on Aging,
Grants Management Division,
Washington, DC 20201. Attention:
Stephen Daniels.
Submissions by courier, overnight
delivery, delivered in person, etc.
should be addressed to: Department of
Health and Human Services,
Administration on Aging, Grants
Management Division, One
Massachusetts Avenue, NW., Room
4604, Washington, DC 20001. Attention:
Stephen Daniels.
3. Submission Dates and Times
To receive consideration, applications
must be received by the deadline listed
in the DATES section of this Notice.
V. Responsiveness Criteria
Each application submitted will be
screened to determine whether it was
received by the closing date and time.
Applications received by the closing
date and time will be screened for
completeness and conformity with the
requirements outlined in Sections III
and IV of this Notice and the Program
Announcement. Only complete
applications that meet these
requirements will be reviewed and
evaluated competitively.
VI. Application Review Information
Eligible applications in response to
this announcement will be reviewed
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30141
according to the following evaluation
criteria:
• Accomplishments and Problem
Statement—Weight: 30 points
• Approach, Work Plan and
Activities—Weight: 40 points
• Project Outcomes and Evaluation—
Weight: 15 points
• Level of Effort (Organization and
Management; Budget and Resources)—
Weight: 15 points
VII. Agency Contacts
Direct inquiries regarding
programmatic issues to U.S. Department
of Health and Human Services,
Administration on Aging, Center for
Planning and Policy Development,
Attention: Greg Case, Washington, DC
20201. Telephone: (202) 357–3442.
Dated: May 22, 2006.
Josefina G. Carbonell,
Assistant Secretary for Aging.
[FR Doc. E6–8047 Filed 5–24–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Head Start Program Grant
Application and Budget Instrument.
OMB No.: 0970–0207.
Description: The Head Start Bureau is
proposing to renew, without changes,
the Head Start Grant Application and
Budget Instrument, which standardizes
the grant application information that is
requested from all Head Start and Early
Head Start grantees applying for
continuation grants. The application
and budget forms are available on a data
diskette and on the Web at https://
www.acfgabi.com. Completed
applications can be transmitted
electronically to Regional and Central
Offices. The Administration on
Children, Youth and Families believes
that this application document makes
the process of applying for Head Start
program grants more efficient for
applicants.
Respondents: Head Start and Early
Head Start grantees.
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Federal Register / Vol. 71, No. 101 / Thursday, May 25, 2006 / Notices
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
HS Grant and Budget Instrument ....................................................................
1,600
1
33
52,800
Estimated Total Annual Burden
Hours: 52,800.
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:
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: May 18, 2006.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 06–4851 Filed 5–24–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006N–0211]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Guidance for
Industry on Submitting and Reviewing
Complete Responses to Clinical Holds
AGENCY:
Food and Drug Administration,
HHS.
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 collection of information contained
in a guidance for industry entitled
‘‘Submitting and Reviewing Complete
Responses to Clinical Holds.’’ The
guidance describes how to submit a
complete response if an investigational
new drug (IND) application is placed on
clinical hold by FDA.
DATES: Submit written or electronic
comments on the collection of
information by July 24, 2006.
ADDRESSES: Submit electronic
comments on the collection to: https://
www.fda.gov/dockets/ecomments.
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:
Karen Nelson, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301– 827–1482.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
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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
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.
Guidance for Industry: Submitting and
Reviewing Complete Responses to
Clinical Holds (OMB Control Number
0910–0445)—Extension
Section 117 of the Food and Drug
Administration Modernization Act
(Public Law 105–115), signed into law
by the President on November 21, 1997,
provides that a written request to FDA
from the applicant of an investigation
that a clinical hold be removed shall
receive a decision in writing, specifying
the reasons for that decision, within 30
days after receipt of such request. A
clinical hold is an order issued by FDA
to the applicant to delay a proposed
clinical investigation or to suspend an
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[Federal Register Volume 71, Number 101 (Thursday, May 25, 2006)]
[Notices]
[Pages 30141-30142]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-4851]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: Head Start Program Grant Application and Budget Instrument.
OMB No.: 0970-0207.
Description: The Head Start Bureau is proposing to renew, without
changes, the Head Start Grant Application and Budget Instrument, which
standardizes the grant application information that is requested from
all Head Start and Early Head Start grantees applying for continuation
grants. The application and budget forms are available on a data
diskette and on the Web at https://www.acfgabi.com. Completed
applications can be transmitted electronically to Regional and Central
Offices. The Administration on Children, Youth and Families believes
that this application document makes the process of applying for Head
Start program grants more efficient for applicants.
Respondents: Head Start and Early Head Start grantees.
[[Page 30142]]
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
HS Grant and Budget Instrument.............. 1,600 1 33 52,800
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 52,800.
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: 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: May 18, 2006.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 06-4851 Filed 5-24-06; 8:45 am]
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