Submission for OMB Review; Comment Request; NIH Intramural Research Training Program Applications, 42899-42900 [E9-20439]
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42899
Federal Register / Vol. 74, No. 163 / Tuesday, August 25, 2009 / Notices
Denning, Office of Governmentwide
Policy, Office of Travel, Transportation,
and Asset Management, at (202) 208–
7642, or by e-mail at https://
www.gsa.gov/perdiemquestions. Please
cite Notice of Per Diem Bulletin 10–01.
SUPPLEMENTARY INFORMATION:
for the development of an HIV testing
social marketing campaign for African
American MSM, a CDC-sponsored social
marketing campaign aimed at increasing
HIV testing rates among young, African
American MSM. The study entails
conducting interviews with a sample of
African American MSM, ages 18 to 44
to: (1) Explore participants’ knowledge,
attitudes and beliefs about HIV and HIV
testing to inform the development of
campaign messages; (2) identify the
most motivating approach, supporting
data, and key messages for materials
development; (3) test creative concepts,
potential campaign themes, logos and
names; and (4) test creative materials
developed based on the findings from
the previous phases of the research.
Findings from this study will be used by
CDC and its partners to inform current
and future program activities. Changes
to the previous approved data collection
consist of a change in the target
audience from African American
heterosexual men to African American
Men who have sex with men. Instead of
a combination of interviews and focus
groups, now only interviews will be
conducted.
A total of 288 participants will be
screened for eligibility in 12 cities with
high incidence and prevalence of HIV.
Of the participants screened, 144 men
will complete individual interviews and
a short paper and pencil survey.
Appropriate consent processes will be
used to obtain verbal consent at the
screening and interview phases of this
study. The Institutional Review Board at
CDC has approved the revised study.
There are no costs to the respondents
other than their time. The total
annualized burden hours are 228.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency Forms Undergoing Paperwork
Reduction Act Review
A. Background
After an analysis of current data, GSA
has determined that current lodging
rates for certain localities do not
adequately reflect the lodging
economics in those areas. GSA used the
same lodging rate setting methodology
for establishing the FY 2010 per diem
rates as when establishing the FY 2009
rates.
B. Change in Standard Procedure
GSA issues/publishes the CONUS per
diem rates, formerly published in
Appendix A to 41 CFR Chapter 301,
solely on the Internet at https://
www.gsa.gov/perdiem. This process,
implemented in 2003, ensures more
timely changes in per diem rates
established by GSA for Federal
employees on official travel within
CONUS. Notices published periodically
in the Federal Register, such as this
one, now constitute the only
notification of revisions in CONUS per
diem rates to agencies.
Dated: August 20, 2009.
Becky Rhodes,
Deputy Associate Administrator.
[FR Doc. E9–20504 Filed 8–21–09; 4:15 pm]
BILLING CODE 6820–14–P
Centers for Disease Control and
Prevention
[30Day-09–0762]
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an
e-mail to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Formative Research to Inform an HIV
Testing Social Marketing Campaign for
African American Men Who Have Sex
with Men (MSM), formally known as
Formative Research to Inform an HIV
Testing Social Marketing Campaign for
African American Heterosexual Men
[OMB No. 0920–0762] [exp. 01/31/
2011]—Revision—National Center for
HIV/AIDS, Viral Hepatitis, Sexually
Transmitted Diseases, and Tuberculosis
Elimination Programs (NCHHSTP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The purpose of the proposed revised
study is to conduct formative research
ESTIMATE OF ANNUALIZED BURDEN TABLE
Form name
African American MSM ...................................
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Type of
respondents
Screener .........................................................
Interview .........................................................
Paper and Pencil Survey ...............................
Dated: August 19, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E9–20374 Filed 8–24–09; 8:45 am]
BILLING CODE P
Number of
respondents
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review;
Comment Request; NIH Intramural
Research Training Program
Applications
Summary: Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the Office of the
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22:52 Aug 24, 2009
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288
144
144
Number of
responses per
respondent
1
1
1
Average
burden
per response
(in hours)
10/60
1
15/60
Director (OD), the National Institutes of
Health (NIH) has submitted to the Office
of Management and Budget (OMB) a
request for review and approval of the
information collection listed below.
This proposed information collection
was previously published in the Federal
Register on June 16, 2009 (Volume 74,
Number 114, pages 28501–28502) and
allowed 60 days for public comment. No
public comments were received. The
purpose of this notice is to allow an
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42900
Federal Register / Vol. 74, No. 163 / Tuesday, August 25, 2009 / Notices
additional 30 days for public comment.
The National Institutes of Health may
not conduct or sponsor, and the
respondent is not required to respond
to, an information collection that has
been extended, revised, or implemented
on or after October 1, 1995, unless it
displays a currently valid OMB control
number.
Proposed Collection: Title: NIH
Intramural Research Training Program
Applications. Type of Information
Collection Request: Extension of a
currently approved collection. Need and
Use of Information Collection: The
proposed information collection activity
is necessary in order to determine the
eligibility and quality of potential
awardees for traineeships in ten (10)
NIH intramural research training
programs. Frequency of Response: On
occasion. Affected Public: Individuals
seeking intramural training
opportunities and references for these
individuals. Type of Respondents:
Postdoctoral, predoctoral,
postbaccalaureate, technical, clinical,
and student applicants. The annual
reporting burden is as follows:
Estimated Number of Respondents:
67,631; Estimated Number of Responses
per Respondent: 1.0506; Average
Burden Hours Per Response: 0.9545;
and Estimated Total Annual Burden
Hours Requested: 67,825. The
annualized cost to respondents is
estimated at $2,033,085. There are no
Capital Costs to report. There are no
Operating 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) 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) 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) 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 those who
are to respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Direct Comments to OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to the: Office
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22:52 Aug 24, 2009
Jkt 217001
of Management and Budget, Office of
Regulatory Affairs,
OIRA_submission@omb.eop.gov or by
fax to 202–395–6974, Attention: Desk
Officer for NIH. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and instruments, contact: Marilyn
Tuttleman, M.S., Chief, Project
Clearance Branch, Office of Policy for
Extramural Research Administration
(OPERA), OER, OD, NIH, One Rockledge
Center, Room 3509, 6705 Rockledge
Drive MSC 7974, Bethesda, MD 20892–
7983, or call non-toll-free number 301–
594–7949 or e-mail your request,
including your address to:
mtuttleman@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30 days of the date of
this publication.
Dated: August 17, 2009.
Steven Alves,
Project Officer, OD, OIR, OITE, National
Institutes of Health.
[FR Doc. E9–20439 Filed 8–24–09; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0380]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Product
Jurisdiction: Assignment of Agency
Component for Review of Premarket
Applications
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 procedure by which an applicant
may obtain an assignment or
designation determination for
combination products.
DATES: Submit written or electronic
comments on the collection of
information by October 26, 2009.
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Fmt 4703
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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:
Jonna Capezzuto, Office of Information
Management (HFA–710), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857,
JonnaLynn.Capezzuto@fda.hhs.gov,
301–796–3794.
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
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.
SUPPLEMENTARY INFORMATION:
E:\FR\FM\25AUN1.SGM
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]]>Agencies
[Federal Register Volume 74, Number 163 (Tuesday, August 25, 2009)]
[Notices]
[Pages 42899-42900]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-20439]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; Comment Request; NIH Intramural
Research Training Program Applications
Summary: Under the provisions of Section 3507(a)(1)(D) of the
Paperwork Reduction Act of 1995, the Office of the Director (OD), the
National Institutes of Health (NIH) has submitted to the Office of
Management and Budget (OMB) a request for review and approval of the
information collection listed below. This proposed information
collection was previously published in the Federal Register on June 16,
2009 (Volume 74, Number 114, pages 28501-28502) and allowed 60 days for
public comment. No public comments were received. The purpose of this
notice is to allow an
[[Page 42900]]
additional 30 days for public comment. The National Institutes of
Health may not conduct or sponsor, and the respondent is not required
to respond to, an information collection that has been extended,
revised, or implemented on or after October 1, 1995, unless it displays
a currently valid OMB control number.
Proposed Collection: Title: NIH Intramural Research Training
Program Applications. Type of Information Collection Request: Extension
of a currently approved collection. Need and Use of Information
Collection: The proposed information collection activity is necessary
in order to determine the eligibility and quality of potential awardees
for traineeships in ten (10) NIH intramural research training programs.
Frequency of Response: On occasion. Affected Public: Individuals
seeking intramural training opportunities and references for these
individuals. Type of Respondents: Postdoctoral, predoctoral,
postbaccalaureate, technical, clinical, and student applicants. The
annual reporting burden is as follows: Estimated Number of Respondents:
67,631; Estimated Number of Responses per Respondent: 1.0506; Average
Burden Hours Per Response: 0.9545; and Estimated Total Annual Burden
Hours Requested: 67,825. The annualized cost to respondents is
estimated at $2,033,085. There are no Capital Costs to report. There
are no Operating 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) 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) 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) 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 those who are to
respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
Direct Comments to OMB: Written comments and/or suggestions
regarding the item(s) contained in this notice, especially regarding
the estimated public burden and associated response time, should be
directed to the: Office of Management and Budget, Office of Regulatory
Affairs, OIRA_submission@omb.eop.gov or by fax to 202-395-6974,
Attention: Desk Officer for NIH. To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact: Marilyn Tuttleman, M.S., Chief, Project Clearance
Branch, Office of Policy for Extramural Research Administration
(OPERA), OER, OD, NIH, One Rockledge Center, Room 3509, 6705 Rockledge
Drive MSC 7974, Bethesda, MD 20892-7983, or call non-toll-free number
301-594-7949 or e-mail your request, including your address to:
mtuttleman@mail.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30 days
of the date of this publication.
Dated: August 17, 2009.
Steven Alves,
Project Officer, OD, OIR, OITE, National Institutes of Health.
[FR Doc. E9-20439 Filed 8-24-09; 8:45 am]
BILLING CODE 4140-01-P
