Board of Scientific Counselors, National Center for Injury Prevention and Control, (BSC, NCIPC), 29754-29755 [2013-12037]
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29754
Federal Register / Vol. 78, No. 98 / Tuesday, May 21, 2013 / Notices
SUMMARY: In accordance with section
10(a)(2) of the Federal Advisory
Committee Act (5 U.S.C. App. 2),
announcement is made of an Agency for
Healthcare Research and Quality
(AHRQ) Special Emphasis Panel (SEP)
meeting on ‘‘Estimating the Costs of
Supporting Primary Care Practice
Transformation (R03)’’.
Dated: May 8, 2013.
Carolyn M. Clancy,
AHRQ Director.
July 11–12, 2013 (Open on July
11 from 8:00 a.m. to 8:30 a.m. and
closed for the remainder of the meeting).
Agency for Healthcare Research and
Quality
DATES:
Hyatt Regency Hotel
Bethesda, One Metro Center, Bethesda,
MD 20814.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Anyone wishing to obtain a roster of
members, agenda or minutes of the nonconfidential portions of this meeting
should contact: Mrs. Bonnie Campbell,
Committee Management Officer, Office
of Extramural Research, Education and
Priority Populations, AHRQ, 540
Gaither Road, Room 2038, Rockville,
Maryland 20850, Telephone: (301) 427–
1554.
Agenda items for this meeting are
subject to change as priorities dictate.
A Special
Emphasis Panel is a group of experts in
fields related to health care research
who are invited by the Agency for
Healthcare Research and Quality
(AHRQ), and agree to be available, to
conduct on an as needed basis,
scientific reviews of applications for
AHRQ support. Individual members of
the Panel do not attend regularlyscheduled meetings and do not serve for
fixed terms or a long period of time.
Rather, they are asked to participate in
particular review meetings which
require their type of expertise.
Substantial segments of the SEP
meeting referenced above will be closed
to the public in accordance with the
provisions set forth in 5 U.S.C. App. 2,
section 10(d), 5 U.S.C. 552b(c)(4), and 5
U.S.C. 552b(c)(6). Grant applications for
‘‘AHRQ RESEARCH SERVICE AWARDS
(NRSA) INSTITUTIONAL RESEARCH
TRAINING GRANTS (T32) Special
Emphasis Award’’ are to be reviewed
and discussed at this meeting. 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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SUPPLEMENTARY INFORMATION:
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Notice of Meetings
Agency for Healthcare Research
and Quality (AHRQ), HHS.
ACTION: Notice of Five AHRQ
Subcommittee Meetings.
AGENCY:
SUMMARY: The subcommittees listed
below are part of AHRQ’s Health
Services Research Initial Review Group
Committee. Grant applications are to be
reviewed and discussed at these
meetings. These meetings will be closed
to the public in accordance with 5
U.S.C. App. 2 section 10(d), 5 U.S.C.
section 552b(c)(4), and 5 U.S.C. section
552b(c)(6).
DATES: See below for dates of meetings:
1. Healthcare Safety and Quality
Improvement Research (HSQR)
Date: June 19–20, 2013 (Open from
8:00 a.m. to 8:30 a.m. on June 19 and
closed for remainder of the meeting)
2. Healthcare Effectiveness and
Outcomes Research (HEOR)
Date: June 19–20, 2013 (Open from
8:00 a.m. to 8:30 a.m. on June 19 and
closed for remainder of the meeting)
3. Healthcare Information Technology
Research (HITR)
Date: June 19–21, 2013 (Open from
8:00 a.m. to 8:30 a.m. on June 19 and
closed for remainder of the meeting)
4. Health Care Research and Training
(HCRT)
Date: June 20, 2013 (Open from 8:00
a.m. to 8:30 a.m. on June 20 and closed
for remainder of the meeting)
5. Health System and Value Research
(HSVR)
Date: July 09–10, 2013 (Open from
8:00 a.m. to 8:30 a.m. on July 09 and
closed for remainder of the meeting)
ADDRESSES: The five meetings will take
place at the following locations:
HSQR, HEOR, HITR, HCRT
Gaithersburg Marriott Washingtonian
Center, 9751 Washingtonian Boulevard,
Gaithersburg, Maryland 20878.
HSVR
Hyatt Regency Hotel Bethesda, One
Metro Center, Bethesda, MD 20814.
FOR FURTHER INFORMATION CONTACT: (To
obtain a roster of members, agenda or
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minutes of the non-confidential portions
of the meetings.)
Mrs. Bonnie Campbell, Committee
Management Officer, Office of
Extramural Research Education and
Priority Populations, AHRQ, 540
Gaither Road, Suite 2000, Rockville,
Maryland 20850, Telephone (301) 427–
1554.
SUPPLEMENTARY INFORMATION: In
accordance with section 10(a)(2) of the
Federal Advisory Committee Act (5
U.S.C. App. 2), AHRQ announces
meetings of the scientific peer review
groups listed above, which are
subcommittees of AHRQ’s Health
Services Research Initial Review Group
Committee. The subcommittee meetings
will be closed to the public in
accordance with the provisions set forth
in 5 U.S.C. App. 2 section 10(d), 5
U.S.C. 552b(c)(4), and 5 U.S.C.
552b(c)(6). 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.
Agenda items for these meetings are
subject to change as priorities dictate.
Dated: May 8, 2013.
Carolyn M. Clancy,
AHRQ Director.
[FR Doc. 2013–11576 Filed 5–20–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Board of Scientific Counselors,
National Center for Injury Prevention
and Control, (BSC, NCIPC)
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 the following meeting of the
aforementioned committee:
Times and Dates:
8:30 a.m.–7:00 p.m., June 13, 2013 (Open).
8:30 a.m.–2:00 p.m., June 14, 2013
(Closed).
Place: CDC, Century Center, 1825 Century
Boulevard NE., Room 1042–1B, Atlanta,
Georgia 30345
Status: Portions of the meeting as
designated above will be closed to the public
in accordance with the 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.
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TKELLEY on DSK3SPTVN1PROD with NOTICES
Federal Register / Vol. 78, No. 98 / Tuesday, May 21, 2013 / Notices
Purpose: The Board will: (1) Conduct,
encourage, cooperate with, and assist other
appropriate public health authorities,
scientific institutions, and scientists in the
conduct of research, investigations,
experiments, demonstrations, and studies
relating to the causes, diagnosis, treatment,
control, and prevention of physical and
mental diseases, and other impairments; (2)
assist States and their political subdivisions
in preventing and suppressing communicable
and non-communicable diseases and other
preventable conditions and in promoting
health and well-being; and (3) conduct and
assist in research and control activities
related to injury.
The Board of Scientific Counselors makes
recommendations regarding policies,
strategies, objectives, and priorities; and
reviews progress toward injury prevention
goals and provides evidence in injury
prevention-related research and programs.
The Board also provides advice on the
appropriate balance of intramural and
extramural research, the structure, progress
and performance of intramural programs. The
Board is designed to provide guidance on
extramural scientific program matters,
including the: (1) Review of extramural
research concepts for funding opportunity
announcements; (2) conduct of Secondary
Peer Review of extramural research grants,
cooperative agreements, and contracts
applications received in response to the
funding opportunity announcements as it
relates to the Center’s programmatic balance
and mission; (3) submission of secondary
review recommendations to the Center
Director of applications to be considered for
funding support; (4) review of research
portfolios, and (5) review of program
proposals.
Matters to be Discussed: The Board of
Scientific Counselors will discuss science
matters to include research strategies needed
to guide the Center’s focus, as well as
updates on the current research portfolio
review and the Pediatric mild-Traumatic
Injury Workgroup. There will be 15 minutes
allotted for public comments at the end of the
open session.
Closed Session: On the second day of the
meeting, the Board will conduct the
Secondary Peer Review of extramural
research grant applications received in
response to Funding Opportunity
Announcement CE–13–002 Research Grants
for Preventing Violence and Violence Related
Injury. Applications will be assessed as it
relates to the Center’s mission and
programmatic balance. The Board will
discuss and vote on the secondary review
recommendations to be provided to the
Center Director for applications to be
considered for funding support.
Agenda items are subject to change as
priorities dictate.
Contact Person for More Information:
Gwendolyn H. Cattledge, Ph.D., M.S.E.H.,
Deputy Associate Director for Science,
NCIPC, CDC, 4770 Buford Highway NE.,
Mailstop F–63, Atlanta, Georgia 30341,
Telephone (770) 488–1430.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
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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. 2013–12037 Filed 5–20–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0473]
Human Immunodeficiency Virus
Patient-Focused Drug Development
and Human Immunodeficiency Virus
Cure Research: Public Meeting
AGENCY:
Food and Drug Administration,
HHS.
Notice of public meeting;
request for comments.
ACTION:
SUMMARY: The Food and Drug
Administration (FDA) is announcing a
public meeting and an opportunity for
public comment on human
immunodeficiency virus (HIV) PatientFocused Drug Development and HIV
Cure Research. Patient-Focused Drug
Development is part of FDA’s
performance commitments in the fifth
authorization of the Prescription Drug
User Fee Act (PDUFA V). FDA is
interested in obtaining patient input on
the impact of HIV on daily life, available
therapies to treat the condition, and
patients’ views on issues related to HIV
cure research, such as perceived
benefits and acceptable risks for
participating in HIV cure research and
clear communication of benefits and
risks through informed consent.
DATES: The public meeting will be held
on Friday, June 14, 2013, from 9:30 a.m.
to 5:30 p.m. Registration to attend the
meeting must be received by
Wednesday, June 5, 2013. Submit
electronic or written comments by July
14, 2013. See the SUPPLEMENTARY
INFORMATION section for information on
how to register for the meeting.
ADDRESSES: The meeting will be held at
the FDA White Oak Campus, 10903
New Hampshire Ave., Building 31
Conference Center, in section A of the
Great Room (Room 1503), Silver Spring,
MD 20993. Entrance for the public
meeting participants is through Building
1, where routine security check
procedures will be performed. For
parking and security information, please
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29755
refer to https://www.fda.gov/AboutFDA/
WorkingatFDA/BuildingsandFacilities/
WhiteOakCampusInformation/
ucm241740.htm.
Submit electronic comments to
www.regulations.gov. Submit written
comments to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FDA will post the complete agenda
and additional meeting background
material approximately 5 days before
the meeting at: https://www.fda.gov/
ForIndustry/UserFees/
PrescriptionDrugUserFee/
ucm348598.htm.
FOR FURTHER INFORMATION CONTACT:
Pujita Vaidya, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, Rm. 1199,
Silver Spring, MD 20993, 301–796–
0684, FAX: 301–847–8443, email:
Pujita.Vaidya@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background on Patient-Focused Drug
Development
FDA has selected HIV to be the focus
of a meeting under Patient-Focused
Drug Development, an initiative that
involves obtaining a better
understanding of patients’ perspectives
on the severity of the disease and the
available therapies for the condition.
Patient-Focused Drug Development is
being conducted to fulfill FDA
performance commitments made as part
of the authorization of PDUFA under
Title I of the Food and Drug Safety and
Innovation Act (FDASIA) (Pub. L. 112–
144). The full set of performance
commitments is available on the FDA
Web site at https://www.fda.gov/
downloads/forindustry/userfees/
prescriptiondruguserfee/
ucm270412.pdf.
FDA has committed to obtain the
patient perspective in 20 disease areas
during the course of PDUFA V. For each
disease area, the Agency will conduct a
public meeting to discuss the disease
and its impact on patients’ daily lives,
the types of treatment benefit that
matter most to patients, and patients’
perspectives on the adequacy of the
available therapies. These meetings will
include participation of FDA review
divisions, the relevant patient
community, and other interested
stakeholders.
In the Federal Register of April 11,
2013 (78 FR 21613), FDA published a
document that announced the disease
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Agencies
[Federal Register Volume 78, Number 98 (Tuesday, May 21, 2013)]
[Notices]
[Pages 29754-29755]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-12037]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Board of Scientific Counselors, National Center for Injury
Prevention and Control, (BSC, NCIPC)
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 the following meeting of the aforementioned
committee:
Times and Dates:
8:30 a.m.-7:00 p.m., June 13, 2013 (Open).
8:30 a.m.-2:00 p.m., June 14, 2013 (Closed).
Place: CDC, Century Center, 1825 Century Boulevard NE., Room
1042-1B, Atlanta, Georgia 30345
Status: Portions of the meeting as designated above will be
closed to the public in accordance with the 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.
[[Page 29755]]
Purpose: The Board will: (1) Conduct, encourage, cooperate with,
and assist other appropriate public health authorities, scientific
institutions, and scientists in the conduct of research,
investigations, experiments, demonstrations, and studies relating to
the causes, diagnosis, treatment, control, and prevention of
physical and mental diseases, and other impairments; (2) assist
States and their political subdivisions in preventing and
suppressing communicable and non-communicable diseases and other
preventable conditions and in promoting health and well-being; and
(3) conduct and assist in research and control activities related to
injury.
The Board of Scientific Counselors makes recommendations
regarding policies, strategies, objectives, and priorities; and
reviews progress toward injury prevention goals and provides
evidence in injury prevention-related research and programs. The
Board also provides advice on the appropriate balance of intramural
and extramural research, the structure, progress and performance of
intramural programs. The Board is designed to provide guidance on
extramural scientific program matters, including the: (1) Review of
extramural research concepts for funding opportunity announcements;
(2) conduct of Secondary Peer Review of extramural research grants,
cooperative agreements, and contracts applications received in
response to the funding opportunity announcements as it relates to
the Center's programmatic balance and mission; (3) submission of
secondary review recommendations to the Center Director of
applications to be considered for funding support; (4) review of
research portfolios, and (5) review of program proposals.
Matters to be Discussed: The Board of Scientific Counselors will
discuss science matters to include research strategies needed to
guide the Center's focus, as well as updates on the current research
portfolio review and the Pediatric mild-Traumatic Injury Workgroup.
There will be 15 minutes allotted for public comments at the end of
the open session.
Closed Session: On the second day of the meeting, the Board will
conduct the Secondary Peer Review of extramural research grant
applications received in response to Funding Opportunity
Announcement CE-13-002 Research Grants for Preventing Violence and
Violence Related Injury. Applications will be assessed as it relates
to the Center's mission and programmatic balance. The Board will
discuss and vote on the secondary review recommendations to be
provided to the Center Director for applications to be considered
for funding support.
Agenda items are subject to change as priorities dictate.
Contact Person for More Information: Gwendolyn H. Cattledge,
Ph.D., M.S.E.H., Deputy Associate Director for Science, NCIPC, CDC,
4770 Buford Highway NE., Mailstop F-63, Atlanta, Georgia 30341,
Telephone (770) 488-1430.
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. 2013-12037 Filed 5-20-13; 8:45 am]
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