National Institute of Neurological Disorders and Stroke; Notice of Meeting, 14979 [2011-6453]
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Federal Register / Vol. 76, No. 53 / Friday, March 18, 2011 / Notices
enables wider use, and maintains NHSN
to obtain scientifically valid clinical
performance indices and benchmarks
that promote healthcare quality and
value at the facility, state, and national
levels; (6) conducts applied research to
identify and develop innovative
methods to detect and monitor HAI and
antimicrobial resistance; (7) conducts
special studies and provides national
estimates of targeted, healthcareassociated adverse events, antimicrobial
use and resistance patterns, and the
extent to which prevention and control
safeguards are in use to protect at-risk
patients across the spectrum of
healthcare delivery sites; (8) uses NHSN
and other data sources to conduct
special studies and provide national
estimates of targeted occupational
illnesses and injuries among healthcare
workers and the extent to which
preventive safeguards are in use across
the spectrum of healthcare delivery
sites; and (9) leads CDC’s national
adverse drug events surveillance
activities and seeks to translate
population-based surveillance data into
evidence-based policies and targeted,
innovative and collaborative
interventions.
Immunization Safety Office (CVLDE).
(1) Assesses the safety of new and
currently available vaccines received by
children, adolescents and adults; (2)
coordinates vaccine safety activities at
CDC; (3) conducts public health
surveillance to identify adverse events
following immunization; (4) in
collaboration with the Food and Drug
Administration, coordinates and
maintains the Vaccine Adverse Event
Reporting System, a national reporting
system that serves as an early-warning
system to detect medical problems that
may be related to vaccines; (5)
coordinates and maintains the Vaccine
Safety Datalink, a collaborative effort
with managed care organizations, to
assess adverse events following
immunization; (6) administers the
Clinical Immunization Safety
Assessment network, a national network
of medical research centers with
expertise in immunization safety
conducting clinical research on
immunization-associated health risks;
(7) participates in the Brighton
Collaboration, an international
collaboration of scientists from around
the world working to develop, evaluate,
and disseminate globally accepted
standard case definitions for adverse
events following immunization and
guidelines for collection, analysis, and
presentation of vaccine safety data; and
(8) works with other federal agencies,
state governments, and other public and
VerDate Mar<15>2010
18:30 Mar 17, 2011
Jkt 223001
private organizations to assess and
promote the safety of vaccines.
Dated: March 10, 2011.
James D. Seligman,
Acting Chief Operating Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2011–6179 Filed 3–17–11; 8:45 am]
BILLING CODE 4160–18–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Neurological
Disorders and Stroke; Notice of
Meeting
Pursuant to section 10(a) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the
Muscular Dystrophy Coordinating
Committee (MDCC).
The meeting 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
inform the Contact Person listed below
in advance of the meeting.
Name of Committee: Muscular Dystrophy
Coordinating Committee.
Date: April 20, 2011.
Time: 8 a.m. to 4:30 p.m.
Agenda: The 2011 meeting of the MDCC
will review Federal agency activities in the
muscular dystrophies, brief participants on
the NIH grant database, NIH RePORTER,
discuss therapy development resources at the
NIH, and review joint NIH/FDA activities
and initiatives in rare diseases. The MDCC
will also discuss new opportunities in
therapy development based upon a
representative example of a new mechanistic
finding and the lessons learned in current
drug development programs. A panel will
review and discuss the challenges of
conducting clinical trials in the muscular
dystrophies.
An agenda will be posted prior to the
meeting on the MDCC Web site: https://
www.ninds.nih.gov/find_people/groups/
mdcc/index.htm.
Place: Hilton Rockville Hotel & Executive
Meeting Center, 1750 Rockville Pike,
Rockville, Maryland 20852–1699.
Contact Person: John D. Porter, PhD,
Executive Secretary, Muscular Dystrophy
Coordinating Committee, National Institute
of Neurological Disorders and Stroke, NIH,
6001 Executive Boulevard, NSC 2172,
Bethesda, MD 20892, (301) 496–5739,
porterjo@ninds.nih.gov.
Any interested person may file written
comments with the committee by forwarding
their statement to the Contact Person listed
on this notice. The statement should include
the name, address, telephone number and
when applicable, the business or professional
affiliation of the interested person.
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14979
(Catalogue of Federal Domestic Assistance
Program Nos. 93.853, Clinical Research
Related to Neurological Disorders; 93.854,
Biological Basis Research in the
Neurosciences, National Institutes of Health,
HHS)
Dated: March 11, 2011.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2011–6453 Filed 3–17–11; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Open Meeting Notice
Notice is hereby given that the
National Institutes of Health (NIH),
Department of Health and Human
Services, will hold a scientific
workshop.
Title: ‘‘State of the Knowledge
Workshop on Myalgic
Encephalomyelitis/Chronic Fatigue
Syndrome (ME/CFS) Research’’.
Dates: April 7–8, 2011.
Time: 8 a.m. to 5 p.m.
Place: Building 31, Conference Rooms
6C8/9/10, NIH campus, Bethesda,
Maryland.
Purpose of the Meeting: This
workshop will bring together subject
matter experts who will discuss
multiple aspects of ME/CFS, including
epidemiology, etiology,
pathophysiology, diagnosis, and
treatment. The workshop panelists will
identify gaps in knowledge and
opportunities for advancing biomedical
research.
This workshop is open to the public.
Please note that attendance is limited.
We encourage registration for those
attending in person (see Web address
below). For those unable to attend, the
workshop will be available via NIH
VideoCasting (https://videocast.nih.gov/)
both during and after the event.
Individuals with disabilities who
need reasonable accommodation should
indicate their needs on registration or
contact Infinity Conference Group by
telephone at 703–925–9455, ext. 0, or email at icg@infinityconferences.com.
For more information including an
agenda, registration, and visitor
information, please visit the workshop
Web site: https://
www.infinityconferences.com/
InfiniBase/Templates/157557/
Index.htm.
Contact Person: Dennis Mangan, PhD;
Chair, Trans-NIH ME/CFS Research
Working Group, Office of Research on
E:\FR\FM\18MRN1.SGM
18MRN1
Agencies
[Federal Register Volume 76, Number 53 (Friday, March 18, 2011)]
[Notices]
[Page 14979]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-6453]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
National Institute of Neurological Disorders and Stroke; Notice
of Meeting
Pursuant to section 10(a) of the Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is hereby given of a meeting of the
Muscular Dystrophy Coordinating Committee (MDCC).
The meeting 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 inform the Contact Person listed below in
advance of the meeting.
Name of Committee: Muscular Dystrophy Coordinating Committee.
Date: April 20, 2011.
Time: 8 a.m. to 4:30 p.m.
Agenda: The 2011 meeting of the MDCC will review Federal agency
activities in the muscular dystrophies, brief participants on the
NIH grant database, NIH RePORTER, discuss therapy development
resources at the NIH, and review joint NIH/FDA activities and
initiatives in rare diseases. The MDCC will also discuss new
opportunities in therapy development based upon a representative
example of a new mechanistic finding and the lessons learned in
current drug development programs. A panel will review and discuss
the challenges of conducting clinical trials in the muscular
dystrophies.
An agenda will be posted prior to the meeting on the MDCC Web
site: https://www.ninds.nih.gov/find_people/groups/mdcc/index.htm.
Place: Hilton Rockville Hotel & Executive Meeting Center, 1750
Rockville Pike, Rockville, Maryland 20852-1699.
Contact Person: John D. Porter, PhD, Executive Secretary,
Muscular Dystrophy Coordinating Committee, National Institute of
Neurological Disorders and Stroke, NIH, 6001 Executive Boulevard,
NSC 2172, Bethesda, MD 20892, (301) 496-5739,
porterjo@ninds.nih.gov.
Any interested person may file written comments with the
committee by forwarding their statement to the Contact Person listed
on this notice. The statement should include the name, address,
telephone number and when applicable, the business or professional
affiliation of the interested person.
(Catalogue of Federal Domestic Assistance Program Nos. 93.853,
Clinical Research Related to Neurological Disorders; 93.854,
Biological Basis Research in the Neurosciences, National Institutes
of Health, HHS)
Dated: March 11, 2011.
Jennifer S. Spaeth,
Director, Office of Federal Advisory Committee Policy.
[FR Doc. 2011-6453 Filed 3-17-11; 8:45 am]
BILLING CODE 4140-01-P