Proposed Collection; 60-Day Comment Request; The Impact of Clinical Research Training and Medical Education at the Clinical Center on Physician Careers in Academia and Clinical Research (CC), 77647-77648 [2015-31631]
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Federal Register / Vol. 80, No. 240 / Tuesday, December 15, 2015 / Notices
Direct Your Comments to
OMB: Send your comments and
suggestions regarding the proposed
information collection contained in this
notice, especially regarding the
estimated public burden and associated
response time to: Office of Management
and Budget, Office of Regulatory Affairs,
New Executive Office Building, Room
10235, Washington, DC 20503,
Attention: Desk Officer for IHS.
FOR FURTHER INFORMATION CONTACT: To
request additional information, please
contact Tamara Clay by one of the
following methods:
• Mail: Tamara Clay, Information
Collection Clearance Officer, Indian
Health Service, Office of Management
Services, Division of Regulatory Affairs,
5600 Fishers Lane, Rockville, Mail Stop
09E70, MD 20857.
• Phone: 301–443–4750.
• Email: Tamara.Clay@ihs.gov.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
Corrections
In the Federal Register of November
17, in FR Doc. 2015–29251, on page
71814, in the middle column, under the
heading Comment Due Date, the due
date is corrected to read as January 9,
2016.
Dated: December 4, 2015.
Robert G. McSwain,
Principal Deputy Director, Indian Health
Service.
Implementation Cooperative Agreement
(U01).
Date: January 22, 2016.
Time: 10:00 a.m. to 1:00 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: Paul A. Amstad, Ph.D.,
Scientific Review Officer, Scientific Review
Program, Division of Extramural Activities,
Room 3G41, NIAID/NIH/DHHS, 5601 Fishers
Lane, Bethesda, MD 20892–7616, 240–669–
5067, pamstad@niaid.nih.gov.
Name of Committee: National Institute of
Allergy and Infectious Diseases Special
Emphasis Panel, NIAID Investigator Initiated
Program Project Applications (P01).
Date: January 22, 2016.
Time: 1:00 p.m. to 5:00 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: Paul A. Amstad, Ph.D.,
Scientific Review Officer, Scientific Review
Program, Division of Extramural Activities,
Room 3G41, NIAID/NIH/DHHS, 5601 Fishers
Lane, Bethesda, MD 20892–7616, 240–669–
5067, pamstad@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)
Dated: December 9, 2015.
Natasha M. Copeland,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–31534 Filed 12–14–15; 8:45 am]
BILLING CODE 4165–16–P
[FR Doc. 2015–31434 Filed 12–14–15; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
asabaliauskas on DSK5VPTVN1PROD with NOTICES
National Institute of Allergy and
Infectious Diseases; Notice of Closed
Meetings
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 meetings.
The meetings 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, NIAID Clinical Trial
VerDate Sep<11>2014
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National Institutes of Health
National Institute of Allergy and
Infectious Diseases; Notice of Closed
Meeting
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.
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Name of Committee: National Institute of
Allergy and Infectious Diseases Special
Emphasis Panel.
Date: January 28, 2016.
Time: 1:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, Room
4H100, 5601 Fishers Lane, Rockville, MD
20892, (Virtual Meeting).
Contact Person: Amir Emanuel Zeituni,
Ph.D., Scientific Review Program, DEA/
NIAID/NIH/DHHS, 5601 Fishers Lane, MSC–
9834, Rockville, MD 20852, 301–496–2550.
(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: December 9, 2015.
Natasha M. Copeland,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–31435 Filed 12–14–15; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment
Request; The Impact of Clinical
Research Training and Medical
Education at the Clinical Center on
Physician Careers in Academia and
Clinical Research (CC)
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
Clinical Center, 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.
To Submit Comments and for Further
Information: Written comments and/or
suggestions from the public and affected
agencies should address 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,
SUMMARY:
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77648
Federal Register / Vol. 80, No. 240 / Tuesday, December 15, 2015 / Notices
mechanical, or other technological
collection techniques or other forms of
information technology. To request
more information on the proposed
project or to obtain a copy of the data
collection plans and instruments,
contact: Robert M. Lembo, MD, Office of
Clinical Research Training and Medical
Education, NIH Clinical Center,
National Institutes of Health, 10 Center
Drive, Room 1N252C, Bethesda, MD
20892–1158, or call non-toll-free
number (301) 496–2636, or Email your
request, including your address to:
robert.lembo@nih.gov. Formal requests
for additional plans and instruments
must be requested in writing.
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.
Proposed Collection: The Impact of
Clinical Research Training and Medical
Education at the Clinical Center on
Physician Careers in Academia and
Clinical Research, Revision OMB#0925–
0602 Expiration Date: 3/31/16, Clinical
Center (CC), National Institutes of
Health (NIH).
Need and Use of Information
Collection: The information collected
will allow continued assessment of the
value of the training provided by the
Office of Clinical Research Training and
Medical Education (OCRTME) at the
NIH Clinical Center and the extent to
which this training promotes (a) patient
safety; (b) research productivity and
independence; and (c) future career
Estimated number
of respondents
Type of respondents
Estimated number
of responses per
respondent
515
415
30
1
1
1
Doctoral Level ..........................................................................
Students ...................................................................................
Other ........................................................................................
Dated: December 7, 2015.
Laura Lee,
Project Clearance Liaison, Warren Grant
Magnuson Clinical Center, National Institutes
of Health.
[FR Doc. 2015–31631 Filed 12–14–15; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
asabaliauskas on DSK5VPTVN1PROD with NOTICES
National Institute of Allergy and
Infectious Diseases; Notice of
Meetings
Pursuant to section 10(a) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of meetings of the AIDS
Research Advisory Committee, NIAID.
The meetings will be open to the
public, with attendance limited to space
available. Individuals who plan to
attend and need special assistance, such
as sign language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
Name of Committee: AIDS Research
Advisory Committee, NIAID.
Date: January 25, 2016.
Time: 1:00 p.m. to 5:00 p.m.
Agenda: Reports from the Division Director
and other staff.
Place: National Institutes of Health,
Natcher Building, Conference Rooms E1/E2,
45 Center Drive, Bethesda, MD 20892.
VerDate Sep<11>2014
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development within clinical,
translational, and academic research
settings. The information received from
respondents is presented to, evaluated
by, and incorporated into the ongoing
operational improvement efforts of the
Director of the Office of Clinical
Research Training and Education, and
the Clinical Center Director. This
information will enable the ongoing
operational improvement efforts of the
OCRTME and its commitment to
providing clinical research training and
medical education of the highest quality
to each trainee.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours:
320.
Contact Person: Mark A. Mueller,
Executive Secretary, AIDS Research Advisory
Committee Division of AIDS, NIAID/NIH,
5601 Fishers Lane, RM 8D39 Bethesda, MD
20892, 301–402–2308, mark.mueller@
nih.gov.
Name of Committee: AIDS Research
Advisory Committee, NIAID.
Date: June 6, 2016.
Time: 1:00 p.m. to 5:00 p.m.
Agenda: Reports from the Division Director
and other staff.
Place: National Institutes of Health,
Natcher Building, Conference Rooms E1/E2,
45 Center Drive, Bethesda, MD 20892.
Contact Person: Mark A. Mueller,
Executive Secretary, AIDS Research Advisory
Committee, Division of AIDS, NIAID/NIH,
5601 Fishers Lane, RM 8D39 Bethesda, MD
20892, 301–402–2308, mark.mueller@
nih.gov.
Name of Committee: AIDS Research
Advisory Committee, NIAID.
Date: September 12, 2016.
Time: 1:00 p.m. to 5:00 p.m.
Agenda: Reports from the Division Director
and other staff.
Place: National Institutes of Health,
Natcher Building, Conference Rooms E1/E2,
45 Center Drive, Bethesda, MD 20892.
Contact Person: Mark A. Mueller,
Executive Secretary, AIDS Research Advisory
Committee, Division of AIDS, NIAID/NIH,
5601 Fishers Lane, Rm 8D39 Bethesda, MD
20892, 301–402–2308, mark.mueller@
nih.gov.
In the interest of security, NIH has
instituted stringent procedures for entrance
onto the NIH campus. All visitor vehicles,
including taxicabs, hotel, and airport shuttles
will be inspected before being allowed on
campus. Visitors will be asked to show one
form of identification (for example, a
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Average burden
hours per
response
Estimated total
annual burden
hours requested
20/60
20/60
20/60
172
138
10
government-issued photo ID, driver’s license,
or passport) and to state the purpose of their
visit.
(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: December 8, 2015.
Natasha Copeland,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–31436 Filed 12–14–15; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HOMELAND
SECURITY
Federal Emergency Management
Agency
[Internal Agency Docket No. FEMA–4245–
DR; Docket ID FEMA–2015–0002]
Texas; Major Disaster and Related
Determinations
Federal Emergency
Management Agency, DHS.
ACTION: Notice.
AGENCY:
This is a notice of the
Presidential declaration of a major
disaster for the State of Texas (FEMA–
4245–DR), dated November 25, 2015,
and related determinations.
DATES: Effective Date: November 25,
2015.
SUMMARY:
E:\FR\FM\15DEN1.SGM
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[Federal Register Volume 80, Number 240 (Tuesday, December 15, 2015)]
[Notices]
[Pages 77647-77648]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-31631]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment Request; The Impact of
Clinical Research Training and Medical Education at the Clinical Center
on Physician Careers in Academia and Clinical Research (CC)
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 Clinical Center, 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.
To Submit Comments and for Further Information: Written comments
and/or suggestions from the public and affected agencies should address
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,
[[Page 77648]]
mechanical, or other technological collection techniques or other forms
of information technology. To request more information on the proposed
project or to obtain a copy of the data collection plans and
instruments, contact: Robert M. Lembo, MD, Office of Clinical Research
Training and Medical Education, NIH Clinical Center, National
Institutes of Health, 10 Center Drive, Room 1N252C, Bethesda, MD 20892-
1158, or call non-toll-free number (301) 496-2636, or Email your
request, including your address to: robert.lembo@nih.gov. Formal
requests for additional plans and instruments must be requested in
writing.
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.
Proposed Collection: The Impact of Clinical Research Training and
Medical Education at the Clinical Center on Physician Careers in
Academia and Clinical Research, Revision OMB#0925-0602 Expiration Date:
3/31/16, Clinical Center (CC), National Institutes of Health (NIH).
Need and Use of Information Collection: The information collected
will allow continued assessment of the value of the training provided
by the Office of Clinical Research Training and Medical Education
(OCRTME) at the NIH Clinical Center and the extent to which this
training promotes (a) patient safety; (b) research productivity and
independence; and (c) future career development within clinical,
translational, and academic research settings. The information received
from respondents is presented to, evaluated by, and incorporated into
the ongoing operational improvement efforts of the Director of the
Office of Clinical Research Training and Education, and the Clinical
Center Director. This information will enable the ongoing operational
improvement efforts of the OCRTME and its commitment to providing
clinical research training and medical education of the highest quality
to each trainee.
OMB approval is requested for 3 years. There are no costs to
respondents other than their time. The total estimated annualized
burden hours: 320.
----------------------------------------------------------------------------------------------------------------
Estimated number Average burden Estimated total
Type of respondents Estimated number of responses per hours per annual burden
of respondents respondent response hours requested
----------------------------------------------------------------------------------------------------------------
Doctoral Level...................... 515 1 20/60 172
Students............................ 415 1 20/60 138
Other............................... 30 1 20/60 10
----------------------------------------------------------------------------------------------------------------
Dated: December 7, 2015.
Laura Lee,
Project Clearance Liaison, Warren Grant Magnuson Clinical Center,
National Institutes of Health.
[FR Doc. 2015-31631 Filed 12-14-15; 8:45 am]
BILLING CODE 4140-01-P