30 Day Federal Register Notice

30 Day FRN 00012017-02472.pdf

PHS Applications and Pre-award Related Reporting (OD)

30 Day Federal Register Notice

OMB: 0925-0001

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9573

Federal Register / Vol. 82, No. 24 / Tuesday, February 7, 2017 / Notices
challenging research activities.
Oversight systems and tools are critical
for the NIH to ensure participant safety,
data integrity, and accountability of the
use of public funds. The NIH has been
engaged in a multi-year effort to
examine how clinical trials are
supported and the level of oversight
needed. The collection of more

structured information in the PHS
applications and pre-award reporting
requirements as well as continued
monitoring and update during the postaward reporting requirements will
facilitate the NIH’s oversight of clinical
trials. In addition, some of the data
reported in the RPPR will ultimately be
accessible to investigators to update

certain sections of forms when
registering or reporting their trials with
ClinicalTrials.gov.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
519,408.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Information collection forms

Reporting:
PHS 416–7 ...............................................................................................
PHS 6031–1 .............................................................................................
PHS 568 ...................................................................................................
iEdison ......................................................................................................
PHS 2271 .................................................................................................
PHS 2590 .................................................................................................
RPPR—Core Data ....................................................................................
Biosketch (Part of RPPR) .........................................................................
Data Tables (Part of RPPR) .....................................................................
Trainee Diversity Report (Part of RPPR) .................................................
PHS Human Subjects and Clinical Trial Information (Part of RPPR, includes inclusion enrollment report) .......................................................
Publication Reporting ...............................................................................
Final RPPR—Core Data ...........................................................................
Data Tables (Part of Final RPPR) ............................................................
Trainee Diversity Report (Part of Final RPPR) ........................................
PHS Human Subjects and Clinical Trial Information (Part of Final
RPPR, includes inclusion/enrollment) ...................................................
PHS 3734 .................................................................................................
Final Progress Report ..............................................................................
SBIR/STTR Phase II Final Progress Report ............................................

Average
burden per
response
(in hours)

Total annual
burden hours

12,580
1,778
11,180
5,697
22,035
243
32,098
2,544
758
480

1
1
1
1
1
1
1
1
1
1

30/60
20/60
5/60
15/60
15/60
18
8
2
4
15/60

6,290
593
932
1,424
5,509
4,374
256,784
5,088
3,032
120

6,420
97,023
18,000
758
480

1
3
1
1
1

4
5/60
10
4
15/60

25,680
8,085
180,000
3,032
120

3,600
479
2,000
1,330

1
1
1
1

4
30/60
1
1

14,400
240
2,000
1,330

Reporting Burden Total .....................................................................
Recordkeeping:
SBIR/STTR Life Cycle Certification ..........................................................

........................

........................

........................

499,033

1,500

1

15/60

375

Grand Total ................................................................................

........................

........................

........................

519,408

Dated: February 1, 2017.
Lawrence A. Tabak,
Deputy Director, National Institutes of Health.
[FR Doc. 2017–02471 Filed 2–6–17; 8:45 am]

This meeting notice is amended to
change the meeting time to 1:00 p.m.–
5:00 p.m. The meeting is closed to the
public.
Dated: February 1, 2017.
Melanie J. Pantoja,
Program Analyst, Office of Federal Advisory
Committee Policy.

BILLING CODE 4140–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[FR Doc. 2017–02430 Filed 2–6–17; 8:45 am]
BILLING CODE 4140–01–P

National Institutes of Health

Lhorne on DSK30JT082PROD with NOTICES

Number of
responses per
respondent

National Institute of Mental Health;
Amended Notice of Meeting

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

Notice is hereby given of a change in
the meeting of the National Institute of
Mental Health Special Emphasis Panel,
February 03, 2017, 10:00 a.m. to
February 03, 2017, 03:00 p.m., National
Institutes of Health, Neuroscience
Center, 6001 Executive Boulevard,
Rockville, MD, 20852 which was
published in the Federal Register on
January 18, 2017, 82FR5588.

National Institutes of Health

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National Institutes of Health,

HHS.
ACTION:

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Notice.

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Comments regarding this
information collection are best assured
of having their full effect if received
within 30-days of the date of this
publication.

DATES:

Submission for OMB Review; 30-Day
Comment Request PHS Applications
and Pre-Award Reporting
Requirements (OD/OPERA)
AGENCY:

In compliance with the
Paperwork Reduction Act of 1995, 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
November 2, 2016, Volume 81, No. 212,
pages 76368–76370 and allowed 60 days
for public comment. No public
comments were received. The purpose
of this notice is to allow an additional
30 days for public comment.

SUMMARY:

Written comments and/or
suggestions regarding the item(s)
contained in this notice, especially
regarding the estimated public burden

ADDRESSES:

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Federal Register / Vol. 82, No. 24 / Tuesday, February 7, 2017 / Notices

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: Ms. Mikia P.
Currie, Project Clearance Branch, Office
of Policy for Extramural Research
Administration, NIH, Rockledge 1
Building, Suite 350, 6705 Rockledge
Drive, Bethesda, MD 20892–7974, or
call non-toll-free number (301) 435–
0941, or Email your request, including
your address to: trialsinfo@od.nih.gov.

FOR FURTHER INFORMATION CONTACT:

The Office
of the Director, NIH, 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.
In compliance with Section
3507(a)(1)(D) of the Paperwork
Reduction Act (PRA) of 1995, the NIH
has submitted to the Office of
Management and Budget (OMB) a
request for review and approval of the
information collection listed below.
Proposed Collection: Public Health
Service (PHS) Applications and Preaward Reporting Requirements.
Revision, OMB 0925–0001, Expiration
Date 10/31/2018. 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.
This collection includes the proposed

SUPPLEMENTARY INFORMATION:

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. The Venture Capital
Operating Companies (VCOC)
Certification and the Small Business
Innovation Research and Small Business
Technology Transfer (SBIR/STTR)
Funding Agreement Certifications are
used by small business applicants.
Oversight systems and tools are critical
for the NIH to ensure participant safety,
data integrity, and accountability of the
use of public funds. The NIH has been
engaged in a multi-year effort to
examine how clinical trials are
supported and the level of oversight
needed. The collection of more
structured information about proposed
clinical trials in the PHS applications
and pre-award reporting requirements
will facilitate the NIH’s oversight of
clinical trials as well as assist in
understanding where needs in the NIH
research portfolio may exist. In
addition, some of the data collected here
will ultimately be accessible to
investigators to pre-populate certain
sections of forms when registering their
trials with ClinicalTrials.gov.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
2,150,389.

use of a new PHS Human Subjects and
Clinical Trial Information form.
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 (NRSA) 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
Activation Notice; and PHS 6031
Payback Agreement. The PHS 398
(paper and electronic), PHS 416–1, 416–
5, and PHS 6031 are currently approved
under 0925–0001. All forms expire 10/
31/2018. Post-award reporting
requirements are simultaneously
consolidated under 0925–0002, and
include the Research Performance
Progress Report (RPPR). The PHS 398
and SF424 applications are used by
applicants to request federal assistance
funds for traditional investigatorinitiated 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

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

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Information collection forms

PHS 398—Paper .............................................................................................
PHS 398/424—Electronic:
PHS Assignment Request Form ..............................................................
PHS 398 Cover Page Supplement ...........................................................
PHS 398 Modular Budget ........................................................................
PHS 398 Training Budget ........................................................................
PHS 398 Training Subaward Budget Attachment(s) Form ......................
PHS 398 Research Plan ..........................................................................
PHS 398 Research Training Program Plan .............................................
Data Tables ..............................................................................................
PHS 398 Career Development Award Supplemental Form .....................
PHS Human Subjects and Clinical Trial Information (includes inclusion
enrollment report) ..................................................................................
Biosketch (424 Electronic) ........................................................................
PHS Fellowship—Electronic:
PHS Fellowship Supplemental Form (includes F reference letters) ........
PHS Assignment Request Form ..............................................................

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Number of
responses per
respondent

Average
burden per
response
(in hours)

Total annual
burden hours

4,247

1

35

148,645

37,120
74,239
56,693
1,122
561
70,866
1,122
1,515
2,251

1
1
1
1
1
1
1
1
1

30/60
1
1
2
90/60
10
10
4
10

18,560
74,239
56,693
2,244
842
708,660
11,220
6,060
22,510

54,838
80,946

1
1

14
2

767,732
161,892

6,707
3,354

1
1

12.5
30/60

83,838
1,677

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Federal Register / Vol. 82, No. 24 / Tuesday, February 7, 2017 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents

Information collection forms

Total annual
burden hours

PHS Human Subjects and Clinical Trial Information (includes inclusion
enrollment report) ..................................................................................
Biosketch (Fellowship) ..............................................................................
416–1 ........................................................................................................
PHS 416–5 ...............................................................................................
PHS 6031 .................................................................................................
VCOC Certification ...................................................................................
SBIR/STTR Funding Agreement Certification ..........................................

5,030
6,707
29
6,707
6,217
6
1,500

1
1
1
1
1
1
1

14
2
10
5/60
5/60
5/60
15/60

70,420
13,414
290
559
518
1
375

Total Annual Burden Hours ...............................................................

........................

........................

........................

2,150,389

Dated: February 1, 2017.
Lawrence A. Tabak,
Deputy Director, National Institutes of Health.
[FR Doc. 2017–02472 Filed 2–6–17; 8:45 am]
BILLING CODE 4140–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

(Catalogue of Federal Domestic Assistance
Program Nos. 93.859, Pharmacology,
Physiology, and Biological Chemistry
Research; 93.350, B—Cooperative
Agreements; 93.859, Biomedical Research
and Research Training, National Institutes of
Health, HHS)
Dated: February 1, 2017.
David Clary,
Program Analyst, Office of Federal Advisory
Committee Policy.

National Institutes of Health

Lhorne on DSK30JT082PROD with NOTICES

Average
burden per
response
(in hours)

Number of
responses per
respondent

National Center for Advancing
Translational Sciences; Notice of
Closed Meeting

[FR Doc. 2017–02433 Filed 2–6–17; 8:45 am]

Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

BILLING CODE 4140–01–P

Name of Committee: National Center for
Advancing Translational Sciences Special
Emphasis Panel, NTU—Bench Testing
Therapeutic/Indication Pairing Strategies
(UH2/UH3).
Date: March 1–2, 2017.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Room
1066, 6701 Democracy Blvd., Bethesda, MD
20817 (Virtual Meeting).
Contact Person: Barbara J. Nelson, Ph.D.,
Scientific Review Officer, Office of Scientific
Review, National Center for Advancing
Translational Sciences (NCATS), National
Institutes of Health, 6701 Democracy Blvd.,
Democracy 1, Room 1080, Bethesda, MD
20892–4874, 301–435–0806, nelsonbj@
mail.nih.gov.

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National Cancer Institute; Amended
Notice of Meeting
Notice is hereby given of a change in
the meeting of the National Cancer
Institute Special Emphasis Panel,
February 27, 2017, 08:00 a.m. to
February 28, 2017, 12:00 p.m., RitzCarlton Hotel, 1700 Tysons Boulevard,
McLean, VA, 22102 which was
published in the Federal Register on
January 27, 2017, 82 FR 8619.
The meeting notice is amended to
change the name of the meeting to NCI
R03/R21 SEP–4. The meeting is closed
to the public.
Dated: February 1, 2017.
Melanie J. Pantoja,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2017–02432 Filed 2–6–17; 8:45 am]
BILLING CODE 4140–01–P

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Coast Guard
[Docket No. USCG–2017–0020]

Merchant Marine Personnel Advisory
Committee
Coast Guard, Department of
Homeland Security.
ACTION: Notice of Federal Advisory
Committee Meeting.
AGENCY:

The Merchant Marine
Personnel Advisory Committee and its
working groups will meet to discuss
various issues related to the training and
fitness of merchant marine personnel.
The meetings will be open to the public.
DATES: The Merchant Marine Personnel
Advisory Committee and its working
groups are scheduled to meet on
Wednesday, March 22, 2017, from 8
a.m. until 5:30 p.m., and the full
Committee is scheduled to meet on
Thursday, March 23, 2017, from 8 a.m.
until 5:30 p.m. Please note that these
meetings may adjourn early if the
Committee has completed its business.
ADDRESSES: The meetings will be held at
The U.S. Coast Guard Headquarters,
Room 6I10–01–C, 2703 Martin Luther
King Jr. Ave. SE., Stop 7509,
Washington, DC 20593–7509 (https://
www.uscg.mil/baseNCR/pages/visitor_
trans.asp).
Attendees at the U.S. Coast Guard
Headquarters who are U.S. citizens will
be required to pre-register no later than
5 p.m. on March 14, 2017, to be
admitted to the meeting. This preregistration should include your name,
telephone number, and company or
group with which you are affiliated.
Non-US citizens will be required to preregister no later than 5 p.m. on March
01, 2017, to be admitted to the meeting.
This pre-registration should include
name, country of citizenship, passport
and expiration date, or diplomatic
SUMMARY:

National Institutes of Health

PO 00000

DEPARTMENT OF HOMELAND
SECURITY

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