Disease, Disability, and Injury Prevention and Control Special Emphasis Panel (SEP): Initial Review, 13012-13013 [2015-05576]
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Federal Register / Vol. 80, No. 48 / Thursday, March 12, 2015 / Notices
OS specifically requests comments on
(1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
Terry S. Clark,
Deputy Information Collection Clearance
Officer.
[FR Doc. 2015–05624 Filed 3–11–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Cancer Institute; Notice of
Closed Meetings
asabaliauskas on DSK5VPTVN1PROD with NOTICES
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 Cancer
Institute Special Emphasis Panel; NCI
Omnibus R03 & R21 SEP–12.
Date: April 30, 2015.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency Bethesda, One
Bethesda Metro Center, 7400 Wisconsin
Avenue, Bethesda, MD 20814.
Contact Person: Dona Love, Ph.D.
Scientific Review Officer, Special Review
Branch, Division of Extramural Activities,
National Cancer Institute, 9609 Medical
Center Drive, Room 7W236, Bethesda, MD
20850, 240–276–5264, donalove@
mail.nih.gov.
Name of Committee: National Cancer
Institute Special Emphasis Panel; Omnibus
SEP–10.
Date: April 30, 2015.
Time: 9:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Cancer Institute Shady
Grove, 9609 Medical Center Drive, Room
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7W602, Rockville, MD 20850, (Telephone
Conference Call).
Contact Person: Delia Tang, Ph.D.,
Scientific Review Officer, Research Program
Review Branch, Division of Extramural
Activities, National Cancer Institute, 9609
Medical Center Drive, Room 7W602,
Bethesda, MD 20892, 240–276–6456,
tangd@.mail.nih.gov.
Information is also available on the
Institute’s/Center’s home page: https://
deainfo.nci.nih.gov/advisory/sep/sep.htm,
where an agenda and any additional
information for the meeting will be posted
when available.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.392, Cancer Construction;
93.393, Cancer Cause and Prevention
Research; 93.394, Cancer Detection and
Diagnosis Research; 93.395, Cancer
Treatment Research; 93.396, Cancer Biology
Research; 93.397, Cancer Centers Support;
93.398, Cancer Research Manpower; 93.399,
Cancer Control, National Institutes of Health,
HHS)
Dated: March 6, 2015.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
Contact Person for More Information:
M. Chris Langub, Ph.D., Scientific
Review Officer, CDC, 4770 Buford
Highway NE., Mailstop F–80, Atlanta,
Georgia 30341, Telephone: (770) 488–
3585, EEO6@cdc.gov.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2015–05574 Filed 3–11–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
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Centers for Disease Control and
Prevention
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
[FR Doc. 2015–05568 Filed 3–11–15; 8:45 am]
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces a meeting for the initial
review of applications in response to
(FOA) DP15–005, Evaluation of a
Stepped Care Approach for Perinatal
Depression Treatment in Obstetrics and
Gynecology Clinics.
Time and Date: 10:00 a.m.–6:00 p.m.,
April 1, 2015 (Closed).
Place: Teleconference.
Status: The meeting will be closed to
the public in accordance with
provisions set forth in section 552b(c)(4)
and (6), title 5 U.S. C., and the
Determination of the Director,
Management Analysis and Services
Office, CDC, pursuant to Pub. L. 92–463.
Matters for Discussion: The meeting
will include the initial review,
discussion, and evaluation of
applications received in response to
‘‘Evaluation of a Stepped Care Approach
for Perinatal Depression Treatment in
Obstetrics and Gynecology Clinics’’,
DP15–005.
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In accordance with Section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces a meeting for the initial
review of applications in response to
(FOA) DP15–009, Improving
Surveillance and Prevention of Epilepsy
Burden in U.S. Communities.
Time and Date: 10:00 a.m.—6:00 p.m.,
March 31, 2015 (Closed).
Place: Teleconference.
Status: The meeting will be closed to the
public in accordance with provisions set
forth in Section 552b(c)(4) and (6), Title 5
U.S.C., and the Determination of the Director,
Management Analysis and Services Office,
CDC, pursuant to Public Law 92–463.
Matters for Discussion: The meeting will
include the initial review, discussion, and
evaluation of applications received in
response to ‘‘Improving Surveillance and
Prevention of Epilepsy Burden in US
Communities’’, DP15–009.
Contact Person for More Information: M.
Chris Langub, Ph.D., Scientific Review
Officer, CDC, 4770 Buford Highway, NE.,
Mailstop F–80, Atlanta, Georgia 30341,
Telephone: (770) 488–3585, EEO6@cdc.gov.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities, for
both the Centers for Disease Control and
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Federal Register / Vol. 80, No. 48 / Thursday, March 12, 2015 / Notices
Prevention and the Agency for Toxic
Substances and Disease Registry.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2015–05576 Filed 3–11–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment
Request Web-Based Resource for
Youth About Clinical Research (NHLBI)
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
National Heart, Lung and Blood
Institute (NHLBI), 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.
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
SUMMARY:
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.
To Submit Comments and For Further
Information: To obtain a copy of the
data collection plans and instruments,
submit comments in writing, or request
more information on the proposed
project, contact: Ms. Victoria
Pemberton, National Heart, Lung, and
Blood Institute, National Institutes of
Health, 6701 Rockledge Dr., Room 8102,
MSC 7940, Bethesda, MD 20892–7940,
or call non-toll-free number 301–435–
0510, or Email your request, including
your address to
pembertonv@nhlbi.nih.gov. Formal
requests for additional plans and
instruments must be requested in
writing.
Comment 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: Web-based
Resource for Youth about Clinical
Research (NHLBI), 0925-New, National
Heart, Lung, and Blood Institute
(NHLBI), National Institutes of Health
(NIH).
Need and Use of Information
Collection: The purpose and use of the
information collection for this project is
to develop a comprehensive web-based
resource for youth with chronic
illnesses or diseases that will attempt to
increase knowledge, self-efficacy, and
positive attitudes towards participation
in various clinical trials and research.
As a result of the proposed web-based
resource, the knowledge gained from
developing and testing this web-based
resource will ultimately help equip
youth to make informed decisions about
clinical research and increase
DATES:
motivation to participate in that
research. In addition, the knowledge
gained will be invaluable to the field of
clinical research given the need for
more clinical trials with youth.
Specifically, the proposed web-based
resource will be an interactive,
multimedia, developmentally
appropriate resource for youth to be
educated about pediatric clinical trials.
The resource will be developed for
youth aged 8 to 14 years. The theme of
‘‘investigative cyber-reporting’’ will be
used throughout and will include youth
making a series of decisions about
different aspects of participating in
clinical research studies. Youth will be
tasked with the responsibility of
learning all they can about clinical
research trials in order to facilitate their
knowledge and decision-making
processes. Language typically used in
journalism and design elements
reminiscent of journalism will be
incorporated into the content, design,
and layout of the resource. There are
three main components that will
comprise the web-based resource. These
include an interactive leaning module,
full length video testimonials, and an
electronic comic book. The benefits and
necessities for this particular research
on pediatric clinical trials are congruent
with NHLBI’s research goals and
mission statement: Attempting to assist
in the enhancement of the health of
individuals so that they can live longer
and more fulfilling lives. The current
lack of knowledge surrounding pediatric
clinical trials can be dangerous and
unhealthy towards the lives of youth,
becoming a large public health need.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
164.
ESTIMATES OF HOUR BURDEN
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hours)
Total annual
burden hour
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Form name
Type of respondent
Individual Interview Questionnaire ....
One-to-One Evaluation Questionnaire.
Pre-Post Study Questionnaire ..........
Individual Interviews Study ..............
One-to-One Evaluation Study ..........
9
5
1
1
2
2
18
10
Pre-Post Feedback Study ................
34
1
4
136
Dated: February 23, 2015.
Lynn Susulske,
NHLBI Project Clearance Liaison, National
Institutes of Health.
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[Federal Register Volume 80, Number 48 (Thursday, March 12, 2015)]
[Notices]
[Pages 13012-13013]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-05576]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Disease, Disability, and Injury Prevention and Control Special
Emphasis Panel (SEP): Initial Review
In accordance with Section 10(a)(2) of the Federal Advisory
Committee Act (Pub. L. 92-463), the Centers for Disease Control and
Prevention (CDC) announces a meeting for the initial review of
applications in response to (FOA) DP15-009, Improving Surveillance and
Prevention of Epilepsy Burden in U.S. Communities.
Time and Date: 10:00 a.m.--6:00 p.m., March 31, 2015 (Closed).
Place: Teleconference.
Status: The meeting will be closed to the public in accordance
with provisions set forth in Section 552b(c)(4) and (6), Title 5
U.S.C., and the Determination of the Director, Management Analysis
and Services Office, CDC, pursuant to Public Law 92-463.
Matters for Discussion: The meeting will include the initial
review, discussion, and evaluation of applications received in
response to ``Improving Surveillance and Prevention of Epilepsy
Burden in US Communities'', DP15-009.
Contact Person for More Information: M. Chris Langub, Ph.D.,
Scientific Review Officer, CDC, 4770 Buford Highway, NE., Mailstop
F-80, Atlanta, Georgia 30341, Telephone: (770) 488-3585,
EEO6@cdc.gov.
The Director, Management Analysis and Services Office, has been
delegated the authority to sign Federal Register notices pertaining
to announcements of meetings and other committee management
activities, for both the Centers for Disease Control and
[[Page 13013]]
Prevention and the Agency for Toxic Substances and Disease Registry.
Elaine L. Baker,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. 2015-05576 Filed 3-11-15; 8:45 am]
BILLING CODE 4163-18-P