Proposed Collection; Comment Request; Application for the Pharmacology Research Associate Program, 27789-27790 [2010-11857]
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27789
Federal Register / Vol. 75, No. 95 / Tuesday, May 18, 2010 / Notices
of 2008,’’ title IV–E was expanded,
effective with FY 2009, to include a
third program, Guardianship Assistance,
and was further expanded, effective
with FY 2010, to include Tribes, tribal
organizations and consortia as
additional grantees.
Ultimately, the combined effect of
these changes will be to significantly
increase the number of grantees, the
number of grant awards and the
required amount of financial reporting.
In recognition of these substantial
program revisions and to accommodate
these changes, the quarterly financial
report has been revised, redesigned and
re-designated as Form CB–496, the
‘‘Title IV–E Programs Quarterly
Financial Report.’’
The Administration for Children and
Families (ACF) provides Federal
funding at the rate of 50 percent for
most administrative and other related
costs and at enhanced rates ranging
from 55 to 75 percent for training costs
as detailed in Federal statute and
regulations. This form is submitted
quarterly by each State and Tribe to
estimate the funding needs for the
upcoming fiscal quarter and to report
expenditures for the fiscal quarter just
ended. The information collected in this
report is used by this agency to calculate
quarterly Federal grant awards and to
enable oversight of the financial
management of the programs.
Comments concerning these revisions
were received from both Federal and
grantee staffs by the ACF Office of
Grants Management, both directly and
in response to an earlier Federal
Register Notice (74 FR 22749, May 14,
2009) that provided many useful
recommendations and suggestions,
many of which were incorporated into
the final draft product.
Respondents: State and Tribal title
IV–E agencies administering the Foster
Care, Adoption Assistance and
Guardianship Assistance Programs.
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of responses per
respondent
Average burden hours per
response
Total burden
hours
Form CB–496 ..................................................................................................
62
4
17
4,216
Estimated Total Annual Burden
Hours: 4,216
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.
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, 725 17th Street, NW.,
Washington, DC 20503, Attn: Desk
Officer for ACF.
Dated: May 12, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–11814 Filed 5–17–10; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; Application for the
Pharmacology Research Associate
Program
SUMMARY: In compliance with the
requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995,
for opportunity for public comment on
proposed data collection projects, the
National Institute of General Medical
Sciences (NIGMS), the National
Institutes of Health (NIH) will publish
periodic summaries of proposed
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
Proposed Collection: Title:
Application for the Pharmacology
Estimated
number of responses per
respondent
mstockstill on DSKH9S0YB1PROD with NOTICES
Type and number of respondents
Estimated total
responses
Average burden hours per
responses
Estimated total
annual burden
hours
requested
1
1
25
75
8.00
1.75
200
131.25
Applicants, 25 ..................................................................................................
Referees, 75 ....................................................................................................
Total Number of Respondents: 100.
Total Number of Responses: 100.
Total Hours: 331.25.
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The annualized cost to respondents is
estimated at:
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Research Associate Program. Type of
Information Collection Request:
Extension of a currently approved
collection, OMB No. 0925–0378,
expiration date December 31, 2010.
Form Numbers: NIH 2721–1, NIH 2721–
2. Need and Use of Information
Collection: The Pharmacology Research
Associate (PRAT) Program will use the
applicant and referee information to
award opportunities for training and
experience in laboratory or clinical
investigation to individuals with a Ph.D.
degree in pharmacology or a related
science, M.D., or other professional
degree through appointments as PRAT
Fellows at the National Institutes of
Health or the Food and Drug
Administration. The goal of the program
is to develop leaders in pharmacological
research for key positions in academic,
industrial, and Federal research
laboratories. Frequency of Response:
Once a year. Affected Public:
Individuals or households; Businesses
or other for-profit. Type of Respondents:
Applicants and Referees.
The annual reporting burden is as
follows:
Fmt 4703
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Applicants: $10,250.00.
Referees: $6,562.50.
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Federal Register / Vol. 75, No. 95 / Tuesday, May 18, 2010 / Notices
There are no Capital Costs, Operating
costs, and/or Maintenance Costs to
report.
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies are invited
on one or more of the following points:
(1) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
function of the agency, including
whether the information will have
practical utility; (2) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and (4) Minimize the burden
of the collection of information on those
who are to respond, including the use
of appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact Ms. Liz Elliott,
NIGMS, NIH, Natcher Building, Room
2AN–18H, 45 Center Drive, MSC 6200,
Bethesda, MD 20892–6200, or call nontoll-free number 301–594–2755 or email your request, including your
address to: elliotte@nigms.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60 days of the date of
this publication.
Dated: May 10, 2010.
Sally Lee,
Executive Officer, National Institute of
General Medical Sciences, National Institutes
of Health.
[FR Doc. 2010–11857 Filed 5–17–10; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0057]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Guidance for
Industry on How to Submit Information
in Electronic Format to the Center for
Veterinary Medicine Using the FDA
Electronic Submission Gateway
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by June 17,
2010.
To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–6974, or e-mailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0454. Also
include the FDA docket number found
in brackets in the heading of this
document
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., P150–
400B, Rockville, MD 20850, 301–796–
3793.
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUPPLEMENTARY INFORMATION:
Guidance for Industry on How to
Submit Information in Electronic
Format to the Center for Veterinary
Medicine Using the FDA Electronic
Submission Gateway (OMB Control
Number 0910–0454)—Extension
The Center for Veterinary Medicine
(CVM), accepts certain types of
submissions electronically with no
requirement for a paper copy. These
types of documents are listed in public
docket 97S–0251 as required by 21 CFR
11.2. CVM’s ability to receive and
process information submitted
electronically is limited by its current
information technology capabilities and
the requirements of the Electronic
Records; Electronic Signatures final
regulation. CVM’s guidance entitled
‘‘Guidance for Industry: How to Submit
Information in Electronic Format to
CVM Using the FDA Electronic
Submission Gateway’’ outlines general
standards to be used for the submission
of any information by e-mail. The likely
respondents are sponsors for new
animal drug applications.
In the Federal Register of February 5,
2010 (75 FR 6038), FDA published a 60day notice requesting public comment
on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
21 CFR Section/Form 3538
No. of
Respondents
11.2
1 There
Annual Frequency
per Response
40
Hours per
Respondent
Total Annual
Responses2
1.3
52
Total Hours
.08
are no capital costs or operating and maintenance costs associated with this collection of information.
submissions received between January 1, 2008, and December 31, 2008.
mstockstill on DSKH9S0YB1PROD with NOTICES
2 Electronic
The number of respondents in table 1
of this document is the number of
sponsors registered to make electronic
submissions (40). The number of total
annual responses is based on a review
of the actual number of such
submissions made between January 1,
2008, and December 31, 2008 (52 x
hours per response (.08) = 4.2 total
hours).
Dated: May 12, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–11808 Filed 5–17–10; 8:45 am]
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]]>Agencies
[Federal Register Volume 75, Number 95 (Tuesday, May 18, 2010)]
[Notices]
[Pages 27789-27790]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-11857]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment Request; Application for the
Pharmacology Research Associate Program
SUMMARY: In compliance with the requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995, for opportunity for public comment
on proposed data collection projects, the National Institute of General
Medical Sciences (NIGMS), the National Institutes of Health (NIH) will
publish periodic summaries of proposed projects to be submitted to the
Office of Management and Budget (OMB) for review and approval.
Proposed Collection: Title: Application for the Pharmacology
Research Associate Program. Type of Information Collection Request:
Extension of a currently approved collection, OMB No. 0925-0378,
expiration date December 31, 2010. Form Numbers: NIH 2721-1, NIH 2721-
2. Need and Use of Information Collection: The Pharmacology Research
Associate (PRAT) Program will use the applicant and referee information
to award opportunities for training and experience in laboratory or
clinical investigation to individuals with a Ph.D. degree in
pharmacology or a related science, M.D., or other professional degree
through appointments as PRAT Fellows at the National Institutes of
Health or the Food and Drug Administration. The goal of the program is
to develop leaders in pharmacological research for key positions in
academic, industrial, and Federal research laboratories. Frequency of
Response: Once a year. Affected Public: Individuals or households;
Businesses or other for-profit. Type of Respondents: Applicants and
Referees.
The annual reporting burden is as follows:
----------------------------------------------------------------------------------------------------------------
Estimated Estimated
number of Estimated Average burden total annual
Type and number of respondents responses per total hours per burden hours
respondent responses responses requested
----------------------------------------------------------------------------------------------------------------
Applicants, 25................................... 1 25 8.00 200
Referees, 75..................................... 1 75 1.75 131.25
----------------------------------------------------------------------------------------------------------------
Total Number of Respondents: 100.
Total Number of Responses: 100.
Total Hours: 331.25.
The annualized cost to respondents is estimated at:
Applicants: $10,250.00.
Referees: $6,562.50.
[[Page 27790]]
There are no Capital Costs, Operating costs, and/or Maintenance
Costs to report.
Request for Comments: Written comments and/or suggestions from the
public and affected agencies are invited on one or more of the
following points: (1) Evaluate whether the proposed collection of
information is necessary for the proper performance of the function of
the agency, including whether the information will have practical
utility; (2) Evaluate the accuracy of the agency's estimate of the
burden of the proposed collection of information, including the
validity of the methodology and assumptions used; (3) Enhance the
quality, utility, and clarity of the information to be collected; and
(4) Minimize the burden of the collection of information on those who
are to respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact Ms. Liz Elliott, NIGMS, NIH, Natcher Building,
Room 2AN-18H, 45 Center Drive, MSC 6200, Bethesda, MD 20892-6200, or
call non-toll-free number 301-594-2755 or e-mail your request,
including your address to: elliotte@nigms.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 60 days
of the date of this publication.
Dated: May 10, 2010.
Sally Lee,
Executive Officer, National Institute of General Medical Sciences,
National Institutes of Health.
[FR Doc. 2010-11857 Filed 5-17-10; 8:45 am]
BILLING CODE 4140-01-P
