Proposed Collection; 60-Day Comment Request; National Institute of Neurological Disorders and Stroke FITBIR Data Access Request, 64093-64094 [2019-25114]
Download as PDF
<![CDATA[
Federal Register / Vol. 84, No. 224 / Wednesday, November 20, 2019 / Notices
(Catalogue of Federal Domestic Assistance
Program Nos. 93.855, Allergy, Immunology,
and Transplantation Research; 93.856,
Microbiology and Infectious Diseases
Research, National Institutes of Health, HHS)
Dated: November 14, 2019.
Tyeshia M. Roberson,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2019–25115 Filed 11–19–19; 8:45 am]
Dated: November 14, 2019.
Tyeshia M. Roberson,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2019–25112 Filed 11–19–19; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4140–01–P
National Institutes of Health
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Proposed Collection; 60-Day Comment
Request; National Institute of
Neurological Disorders and Stroke
FITBIR Data Access Request
National Institutes of Health
AGENCY:
National Institute of Allergy and
Infectious Diseases; Notice of Closed
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, 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.
Name of Committee: National Institute of
Allergy and Infectious Diseases Special
Emphasis Panel; HIV/AIDS Adult
Therapeutics Clinical Trials Network
Leadership and Operations Center (UM1
Clinical Trial Required).
Date: December 6, 2019.
Time: 11:00 a.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 5601
Fishers Lane, Rockville, MD 20892
(Telephone Conference Call).
Contact Person: J. Bruce Sundstrom, Ph.D.,
Scientific Review Officer, Scientific Review
Program, Division of Extramural Activities,
National Institutes of Health/NIAID, 5601
Fishers Lane, Room 3G11A, MSC 9823,
Bethesda, MD 20892–9823, 240–669–5045,
sundstromj@niaid.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.855, Allergy, Immunology,
and Transplantation Research; 93.856,
Microbiology and Infectious Diseases
Research, National Institutes of Health, HHS)
VerDate Sep<11>2014
17:21 Nov 19, 2019
Jkt 250001
National Institutes of Health,
HHS.
ACTION:
Notice.
In compliance with the
requirement of the Paperwork
Reduction Act of 1995, to provide
opportunity for public comment on
proposed data collection projects, the
National Institute of Neurological
Disorders and Stroke (NINDS), will
publish periodic summaries of proposed
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
DATES: Comments regarding this
information collection are best assured
of having their full effect if received
within 60 days of the date of this
publication.
FOR FURTHER INFORMATION CONTACT: To
obtain a copy of the data collection
plans and instruments, submit
comments in writing, or request more
information on the proposed project,
contact: Dr. Sophia Jeon, Health Science
Policy Analyst, Office of Science Policy
and Planning, OSPP, NINDS, NIH, 31
Center Drive, Building 31, Room 8A03,
Bethesda, MD 20892, or call non-tollfree number (301) 435–7571, or Email
your request, including your address to:
sophia.jeon@nih.gov Formal requests for
additional plans and instruments must
be requested in writing.
SUPPLEMENTARY INFORMATION: Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: written
comments and/or suggestions from the
public and affected agencies are invited
to address 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
SUMMARY:
PO 00000
Frm 00056
Fmt 4703
Sfmt 4703
64093
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.
Proposed Collection Title: National
Institute of Neurological Disorders and
Stroke FITBIR Data Access Request,
0925–0677, REINSTATEMENT with
change–, Expiration Date 12/31/2019
National Institute of Neurological
Disorders and Stroke (NINDS), National
Institutes of Health (NIH).
Need and Use of Information
Collection: The FITBIR Informatics
System Data Access Request form is
necessary for Principal Investigators
(PIs) and their organization or
corporations with approved assurance
from the DHHS Office of Human
Research Protections to access data or
images from the FITBIR Informatics
System for research purposes. The
primary use of this information is to
document, track, monitor, and evaluate
the use of the FITBIR datasets, as well
as to notify interested recipients of
updates, corrections or other changes to
the database. For reinstatement of this
collection, the agency proposes to add
Data Submission Request to allow
‘‘Submitter’’ Principal Investigators (PIs)
to request submission of their data to
the FITBIR database for broad data
sharing and to document, monitor, and
track the FITBIR data submissions.
Types of respondents affected by this
information collection are researchers,
such as ‘‘Recipient’’ PIs who are
interested in obtaining access to study
data and images from the FITBIR
Informatics System for research
purposes, or ‘‘Submitter’’ PIs who are
interested in submitting data to
contribute to the FITBIR database for
their data to be shared with the
traumatic brain injury research
community.
OMB approval reinstatement is
requested for 3 years. There are no costs
to respondents other than their time.
The total estimated annualized burden
hours are 96.
E:\FR\FM\20NON1.SGM
20NON1
64094
Federal Register / Vol. 84, No. 224 / Wednesday, November 20, 2019 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Average
burden per
response
(in hours)
Number of
responses per
respondent
Total annual
burden hours
Form name
Type of respondents
FITBIR Data Access Request ..
Individuals (‘‘Recipient’’ Principal Investigators).
Individuals (‘‘Submitter’’ Principal Investigators).
85
1
60/60
85
65
1
10/60
11
...................................................................
........................
150
........................
96
FITBIR Data Submission Request.
Total ..................................
Dated: November 14, 2019.
Paul Scott,
Project Clearance Liaison, National Institute
of Neurological Disorders and Stroke, NIH.
[FR Doc. 2019–25114 Filed 11–19–19; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Amended
Notice of Meeting
Notice is hereby given of a change in
the meeting of the Center for Scientific
Review Special Emphasis Panel,
November 22, 2019, 11:00 a.m. to 5:00
p.m., at the Center for Scientific Review,
National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
which was published in the Federal
Register on October 30, 2019, 84 FR
58161.
The meeting format of the Special
Emphasis Panel RFA Panel: Tobacco
Regulatory Science B, has been changed
to a Virtual Assisted Meeting. The
meeting date, time and location remain
the same. The meeting is closed to the
public.
Dated: November 15, 2019.
Ronald J. Livingston, Jr.,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2019–25181 Filed 11–19–19; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HOMELAND
SECURITY
Coast Guard
[Docket No. USCG–2019–0878]
Notice of Public Meeting on Consistent
Implementation of Regulation 14.1.3 of
MARPOL Annex VI (Global 0.50%
Sulfur Limit)
Coast Guard, DHS.
Notice of meeting.
AGENCY:
ACTION:
VerDate Sep<11>2014
17:21 Nov 19, 2019
Jkt 250001
The United States Coast
Guard will conduct a public meeting in
Washington, DC on consistent
implementation of regulation 14.1.3 of
MARPOL Annex IV (Global 0.50%
Sulfur Limit). The purpose of this
meeting will be to review the MARPOL
Annex VI provisions for implementing
the Global 0.50% Sulfur Limit and the
associated guidance developed through
the International Maritime Organization,
as well as discuss related issues and
Coast Guard enforcement plans.
DATES: This public meeting will be held
on Thursday, December 5, beginning at
9:30 a.m. and ending at 3:00 p.m.,
Eastern Time. This meeting is open to
the public.
ADDRESSES: The public meeting will be
held in Room 3, located on the first floor
near the main entrance of the United
States Department of Transportation
building in Washington, DC. The United
States Department of Transportation
building is located at 1200 New Jersey
Ave. SE, in Washington, DC, across the
street from the Navy Yard-Ballpark
Metro Station. Due to security
requirements, each visitor must present
a valid government-issued photo
identification (for example, a driver’s
license) in order to gain entrance to the
building. Those desiring to attend the
public meeting should contact the Coast
Guard ahead of the meeting (see FOR
FURTHER INFORMATION CONTACT) to
facilitate the security process related to
building access, or to request reasonable
accommodation.
FOR FURTHER INFORMATION CONTACT: For
additional information about this public
meeting you may contact Mr. Wayne
Lundy by telephone at (202) 372–1379
or by email at Wayne.M.Lundy@
uscg.mil.
SUPPLEMENTARY INFORMATION: Annex VI
to the International Convention for the
Prevention of Pollution from Ships
(MARPOL Annex VI) addresses air
pollution from ships. Regulation 14
addresses particulate matter (PM) and
sulfur oxide (SOX) emissions through
fuel sulfur content limits. Beginning on
January 1, 2015, fuel used in ships
SUMMARY:
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
operating in designated Emission
Control Areas (ECAs), including the
North American and U.S. Caribbean Sea
ECAs, may not exceed 1,000 ppm.
Outside of designated ECAs, the sulfur
content of marine fuel currently may not
exceed 35,000 ppm; this limit will be
reduced to 5,000 ppm beginning on
January 1, 2020.
As required by Regulation 14.8 of
Annex VI, the 2020 global sulfur limit
was reviewed and the limit was
confirmed by the Marine Environment
Protection Committee at its 70th session
in November, 2016. At the 71st session,
the Marine Environment Protection
Committee agreed on a new work output
to consider measures to promote
consistent implementation of the global
sulfur limit to address industry
concerns and promote a level playing
field with regard to compliance and
enforcement of the new standards.
The Coast Guard will conduct a
meeting on Thursday, December 5 at the
United States Department of
Transportation building in Washington,
DC, provide an overview of the
MARPOL Annex VI provisions for
implementing the Global 0.50% Sulfur
Limit and the associated guidance
developed through the International
Maritime Organization. Related issues
will also be discussed, including
enforcement in the United States,
changes to Port State Control
procedures, fuel oil non-availability
notices, Ship Implementation Plans, inuse and onboard fuel oil sampling, and
Exhaust Gas Cleaning Systems.
This meeting is open to the public.
Please note that the public meeting has
a limited number of seats. Also, the
meeting may close early if all business
is finished. Those interested in
attending should contact Mr. Wayne
Lundy by telephone at (202) 372–1379
or by email at Wayne.M.Lundy@
uscg.mil.
Information on Services for Individuals
With Disabilities
For information on facilities or
services for individuals with disabilities
or to request special assistance at the
E:\FR\FM\20NON1.SGM
20NON1
]]>Agencies
[Federal Register Volume 84, Number 224 (Wednesday, November 20, 2019)]
[Notices]
[Pages 64093-64094]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-25114]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment Request; National Institute
of Neurological Disorders and Stroke FITBIR Data Access Request
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement of the Paperwork Reduction
Act of 1995, to provide opportunity for public comment on proposed data
collection projects, the National Institute of Neurological Disorders
and Stroke (NINDS), will publish periodic summaries of proposed
projects to be submitted to the Office of Management and Budget (OMB)
for review and approval.
DATES: Comments regarding this information collection are best assured
of having their full effect if received within 60 days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data
collection plans and instruments, submit comments in writing, or
request more information on the proposed project, contact: Dr. Sophia
Jeon, Health Science Policy Analyst, Office of Science Policy and
Planning, OSPP, NINDS, NIH, 31 Center Drive, Building 31, Room 8A03,
Bethesda, MD 20892, or call non-toll-free number (301) 435-7571, or
Email your request, including your address to: [email protected]
Formal requests for additional plans and instruments must be requested
in writing.
SUPPLEMENTARY INFORMATION: Section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: written comments and/or suggestions
from the public and affected agencies are invited to address 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.
Proposed Collection Title: National Institute of Neurological
Disorders and Stroke FITBIR Data Access Request, 0925-0677,
REINSTATEMENT with change-, Expiration Date 12/31/2019 National
Institute of Neurological Disorders and Stroke (NINDS), National
Institutes of Health (NIH).
Need and Use of Information Collection: The FITBIR Informatics
System Data Access Request form is necessary for Principal
Investigators (PIs) and their organization or corporations with
approved assurance from the DHHS Office of Human Research Protections
to access data or images from the FITBIR Informatics System for
research purposes. The primary use of this information is to document,
track, monitor, and evaluate the use of the FITBIR datasets, as well as
to notify interested recipients of updates, corrections or other
changes to the database. For reinstatement of this collection, the
agency proposes to add Data Submission Request to allow ``Submitter''
Principal Investigators (PIs) to request submission of their data to
the FITBIR database for broad data sharing and to document, monitor,
and track the FITBIR data submissions. Types of respondents affected by
this information collection are researchers, such as ``Recipient'' PIs
who are interested in obtaining access to study data and images from
the FITBIR Informatics System for research purposes, or ``Submitter''
PIs who are interested in submitting data to contribute to the FITBIR
database for their data to be shared with the traumatic brain injury
research community.
OMB approval reinstatement is requested for 3 years. There are no
costs to respondents other than their time. The total estimated
annualized burden hours are 96.
[[Page 64094]]
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total annual
Form name Type of respondents respondents responses per response (in burden hours
respondent hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
FITBIR Data Access Request..................... Individuals (``Recipient'' Principal 85 1 60/60 85
Investigators).
FITBIR Data Submission Request................. Individuals (``Submitter'' Principal 65 1 10/60 11
Investigators).
---------------------------------------------------------------
Total...................................... ....................................... .............. 150 .............. 96
--------------------------------------------------------------------------------------------------------------------------------------------------------
Dated: November 14, 2019.
Paul Scott,
Project Clearance Liaison, National Institute of Neurological Disorders
and Stroke, NIH.
[FR Doc. 2019-25114 Filed 11-19-19; 8:45 am]
BILLING CODE 4140-01-P
