Proposed Collection: Comment Request Post-Award Reporting Requirements Including New Research Performance Progress Report Collection, 13131-13132 [2012-5306]
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Federal Register / Vol. 77, No. 43 / Monday, March 5, 2012 / Notices
Estimated Total Annual Burden
Hours: 6,292.
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 may 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. Email address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection activity—
National Child Abuse and Neglect Data
System.
The Department specifically requests
comments on: (a) The proposed change
to the two data collection instruments—
the Child File and the Agency File; (b)
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;
(c) the quality, utility, and clarity of the
information to be collected; (d) the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information; and (e) 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.
Robert Sargis,
Reports Clearance Officer.
Copies are available from
the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852, 301–827–
6860.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Teresa L. Hays, Advisory Committee
and Oversight Management Staff, Food
and Drug Administration, 10903 New
Hampshire Ave., Silver Spring, MD
20993, 301–796–8220.
Under
section 10(d) of the Federal Advisory
Committee Act (5 U.S.C. app.) and 21
CFR 14.60(d), FDA has filed with the
Library of Congress the annual reports
for the following FDA advisory
committees that held closed meetings
during the period October 1, 2010
through September 30, 2011:
SUPPLEMENTARY INFORMATION:
Center for Biologics Evaluation and
Research
Allergenic Products Advisory
Committee
Blood Products Advisory Committee
Cellular, Tissue and Gene Therapies
Advisory Committee
Vaccines and Related Biological
Products Advisory Committee
Center for Drug Evaluation and
Research
Cardiovascular and Renal Drugs
Advisory Committee
Gastrointestinal Drug Advisory
Committee
National Center for Toxicological
Research
[FR Doc. 2012–5251 Filed 3–2–12; 8:45 am]
Science Board to the National Center for
Toxicological Research
BILLING CODE 4184–01–P
Center for Tobacco Products
Tobacco Products Scientific Advisory
Committee
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0001]
Advisory Committees; Filing of Closed
Meeting Reports
AGENCY:
Food and Drug Administration,
HHS.
erowe on DSK2VPTVN1PROD with NOTICES
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that, as required by the Federal
Advisory Committee Act, the Agency
has filed with the Library of Congress
the annual reports of those FDA
advisory committees that held closed
meetings during fiscal year 2011.
SUMMARY:
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15:06 Mar 02, 2012
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Annual reports are available for
public inspections between 9 a.m. and
4 p.m., Monday through Friday.
• The Library of Congress, Madison
Bldg., Newspaper and Current
Periodical Reading Room, 101
Independence Ave. SE., Rm. 133,
Washington, DC; and
• The Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
Dated: February 23, 2012.
Jill Hartzler Warner,
Acting Associate Commissioner for Special
Medical Programs.
[FR Doc. 2012–5208 Filed 3–2–12; 8:45 am]
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13131
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection: Comment
Request Post-Award Reporting
Requirements Including New Research
Performance Progress Report
Collection
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
Office of the Director, 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: Public
Health Service (PHS) Post-award
Reporting Requirements. Type of
Information Collection Request:
Revision. This collection represents a
consolidation of post-award reporting
requirements under the PRA, and
includes the new Research Performance
Progress Report (RPPR). Need and Use
of Information Collection: The RPPR
will replace existing interim
performance reports used by all NIH,
Food and Drug Administration, Centers
for Disease Control and Prevention, and
Agency for Healthcare Research and
Quality (AHRQ) grantees. Interim
progress reports are required to continue
support of a PHS grant for each budget
year within a competitive segment. The
phased transition to the RPPR requires
the maintenance of dual reporting
processes for a period of time. Thus this
information collection is for the new use
of the RPPR, and continued use of the
PHS Non-competing Continuation
Progress Report (PHS 2590, currently
approved under 0925–0001), and the
NIH AHRQ Ruth L. Kirschstein National
Research Service Award (NRSA)
Individual Fellowship Progress Report
for Continuation Support (PHS 416–9,
currently approved under 0925–0002).
Only one interim progress report (RPPR
or PHS2590/416–9) will be utilized for
any given award. This collection also
includes other PHS post-award
reporting requirements: PHS 416–7
NRSA Termination Notice, PHS 2271
Statement of Appointment, 6031–1
NRSA Annual Payback Activities
Certification, (currently approved under
0925–0002, expiration 6/30/2012); and
HHS 568 Final Invention Statement and
Certification, Final Progress Report
instructions, and iEdison, and PHS 3734
Statement Relinquishing Interests and
Rights in a PHS Research Grant
SUMMARY:
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13132
Federal Register / Vol. 77, No. 43 / Monday, March 5, 2012 / Notices
(currently approved under 0925–0001,
expiration 6/30/2012). The PHS 416–7,
2271, and 6031–1 are used by NRSA
recipients to activate, terminate, and
provide for payback of a NRSA. Closeout of an award requires a Final
Invention Statement (HHS 568) and
Final Progress Report. iEdison allows
grantees and Federal agencies to meet
statutory requirements for reporting
inventions and patents. The PHS 3734
serves as the official record of grantee
relinquishment of a PHS award when an
award is transferred from one grantee
institution to another. Pre-award
reporting requirements are
simultaneously consolidated under
0925–0001. Frequency of response:
Grantees are required to report annually.
Affected Public: Universities and other
research institutions; Business or other
for-profit; Not-for-profit institutions;
Federal Government; and State, Local or
Tribal Government. Type of
Respondents: University administrators
and principal investigators. The annual
reporting burden is as follows: Total
Estimated Number of Respondents:
112,986. Estimated Number of
Responses per Respondent: 1. Average
Burden Hours per Response: 5.6.
Estimated Total Annual Burden Hours
Requested: 640,677. The annualized
cost to respondents is estimated to be
$22,423,709. 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.
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. Mikia Currie,
email: curriem@od.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
VerDate Mar<15>2010
15:06 Mar 02, 2012
Jkt 226001
received within 60-days of the date of
this publication.
Dated: February 28, 2012.
Joe Ellis,
Director, Office of Policy for Extramural
Research Administration, Office of
Extramural Research, National Institutes of
Health.
[FR Doc. 2012–5306 Filed 3–2–12; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection: Comment
Request; Revision ‘‘PHS Applications
and Pre-Award Reporting
Requirements’’
In compliance with the
requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act (PRA) of
1995, for opportunity for public
comment on proposed data collection
projects, the Office of the Director,
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: Public
Health Service (PHS) Applications and
Pre-award Reporting Requirements.
Type of Information Collection Request:
Revision, OMB 0925–0001, Expiration
Date 6/30/2012. Form numbers: PHS
398, PHS416–1, 416–5, and PHS 6031.
This collection represents a
consolidation of PHS applications and
pre-award reporting requirements into a
revised data collection under the PRA.
Need and Use of Information Collection:
This collection includes PHS
applications and pre-award reporting
requirements: PHS 398 [paper] Public
Health Service Grant Application forms
and instructions; PHS 398 [electronic]
PHS Grant Application component
forms and agency specific instructions
used in combination with the SF424
(R&R); PHS Fellowship Supplemental
Form and agency specific instructions
used in combination with the SF424
(R&R) forms/instructions for
Fellowships [electronic]; PHS 416–1
Ruth L. Kirschstein National Research
Service Award Individual Fellowship
Application Instructions and Forms
used only for a change of sponsoring
institution application [paper];
Instructions for a Change of Sponsoring
Institution for NRSA Fellowships (F30,
F31, F32 and F33) and non-NRSA
Fellowships; PHS 416–5 Ruth L.
Kirschstein National Research Service
Award Individual Fellowship
SUMMARY:
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Activation Notice; and PHS 6031
Payback Agreement. The PHS 398
(paper and electronic) is currently
approved under 0925–0001; PHS 416–1,
416–5, and PHS 6031 are currently
approved under 0925–0002. All forms
expire 6/30/2012. Post-award reporting
requirements are simultaneously
consolidated under 0925–XXXX, and
include the new Research Performance
Progress Report (RPPR). The PHS 398
application is used by applicants to
request Federal assistance funds for
traditional investigator-initiated
research projects and to request access
to databases and other PHS resources.
The PHS 416–1 is used only for a
change of sponsoring institution
application. PHS Fellowship
Supplemental Form and agency specific
instructions is used in combination with
the SF424 (R&R) forms/instructions for
Fellowships and is used by individuals
to apply for direct research training
support. Awards are made to individual
applicants for specified training
proposals in biomedical and behavioral
research, selected as a result of a
national competition. The PHS 416–5 is
used by individuals to indicate the start
of their NRSA awards. The PHS 6031
Payback Agreement is used by
individuals at the time of activation to
certify agreement to fulfill the payback
provisions. Frequency of response:
Applicants may submit applications for
published receipt dates. For NRSA
awards, fellowships are activated and
trainees appointed. Affected Public:
Universities and other research
institutions; Business or other for-profit;
Not-for-profit institutions; Federal
Government; and State, Local or Tribal
Government. Type of Respondents:
University administrators and principal
professionals. The annual reporting
burden is as follows: Total Estimated
Number of Respondents: 94,326;
Estimated Number of Responses per
Respondent: 1, Average Burden Hours
Per Response: 21.75; Estimated Total
Annual Burden Hours Requested:
2,051,794. The estimated annualized
cost to respondents is $71,812,769.
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,
E:\FR\FM\05MRN1.SGM
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]]>Agencies
[Federal Register Volume 77, Number 43 (Monday, March 5, 2012)]
[Notices]
[Pages 13131-13132]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-5306]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection: Comment Request Post-Award Reporting
Requirements Including New Research Performance Progress Report
Collection
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 Office of the Director,
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: Public Health Service (PHS) Post-award
Reporting Requirements. Type of Information Collection Request:
Revision. This collection represents a consolidation of post-award
reporting requirements under the PRA, and includes the new Research
Performance Progress Report (RPPR). Need and Use of Information
Collection: The RPPR will replace existing interim performance reports
used by all NIH, Food and Drug Administration, Centers for Disease
Control and Prevention, and Agency for Healthcare Research and Quality
(AHRQ) grantees. Interim progress reports are required to continue
support of a PHS grant for each budget year within a competitive
segment. The phased transition to the RPPR requires the maintenance of
dual reporting processes for a period of time. Thus this information
collection is for the new use of the RPPR, and continued use of the PHS
Non-competing Continuation Progress Report (PHS 2590, currently
approved under 0925-0001), and the NIH AHRQ Ruth L. Kirschstein
National Research Service Award (NRSA) Individual Fellowship Progress
Report for Continuation Support (PHS 416-9, currently approved under
0925-0002). Only one interim progress report (RPPR or PHS2590/416-9)
will be utilized for any given award. This collection also includes
other PHS post-award reporting requirements: PHS 416-7 NRSA Termination
Notice, PHS 2271 Statement of Appointment, 6031-1 NRSA Annual Payback
Activities Certification, (currently approved under 0925-0002,
expiration 6/30/2012); and HHS 568 Final Invention Statement and
Certification, Final Progress Report instructions, and iEdison, and PHS
3734 Statement Relinquishing Interests and Rights in a PHS Research
Grant
[[Page 13132]]
(currently approved under 0925-0001, expiration 6/30/2012). The PHS
416-7, 2271, and 6031-1 are used by NRSA recipients to activate,
terminate, and provide for payback of a NRSA. Close-out of an award
requires a Final Invention Statement (HHS 568) and Final Progress
Report. iEdison allows grantees and Federal agencies to meet statutory
requirements for reporting inventions and patents. The PHS 3734 serves
as the official record of grantee relinquishment of a PHS award when an
award is transferred from one grantee institution to another. Pre-award
reporting requirements are simultaneously consolidated under 0925-0001.
Frequency of response: Grantees are required to report annually.
Affected Public: Universities and other research institutions; Business
or other for-profit; Not-for-profit institutions; Federal Government;
and State, Local or Tribal Government. Type of Respondents: University
administrators and principal investigators. The annual reporting burden
is as follows: Total Estimated Number of Respondents: 112,986.
Estimated Number of Responses per Respondent: 1. Average Burden Hours
per Response: 5.6. Estimated Total Annual Burden Hours Requested:
640,677. The annualized cost to respondents is estimated to be
$22,423,709. 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.
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. Mikia Currie, email: curriem@od.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: February 28, 2012.
Joe Ellis,
Director, Office of Policy for Extramural Research Administration,
Office of Extramural Research, National Institutes of Health.
[FR Doc. 2012-5306 Filed 3-2-12; 8:45 am]
BILLING CODE 4140-01-P
