Decision To Evaluate a Petition To Designate a Class of Employees From Ames Laboratory in Ames, IA, To Be Included in the Special Exposure Cohort, 22900 [2011-9928]
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Federal Register / Vol. 76, No. 79 / Monday, April 25, 2011 / Notices
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Dated: April 19, 2011.
Erin Poetter,
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Technology.
[FR Doc. 2011–9941 Filed 4–22–11; 8:45 am]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institute for
Occupational Safety and Health
(NIOSH), Department of Health and
Human Services (HHS).
AGENCY:
Notice.
HHS gives notice as required
by 42 CFR 83.12(e) of a decision to
evaluate a petition to designate a class
of employees from Ames Laboratory in
Ames, Iowa, to be included in the
Special Exposure Cohort under the
Energy Employees Occupational Illness
Compensation Program Act of 2000. The
initial proposed definition for the class
being evaluated, subject to revision as
warranted by the evaluation, is as
follows:
Facility: Ames Laboratory.
Location: Ames, Iowa.
Job Titles and/or Job Duties: All
Department of Energy (DOE) employees,
its predecessor agencies, and its
contractors and subcontractors who
worked in any area of the DOE facility.
Period of Employment: January 1,
1942 through December 31, 1970.
jdjones on DSKHWCL6B1PROD with NOTICES
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
Stuart L. Hinnefeld, Director, Division
of Compensation Analysis and Support,
National Institute for Occupational
Safety and Health (NIOSH), 4676
Columbia Parkway, MS C–46,
Cincinnati, OH 45226, Telephone 877–
222–7570. Information requests can also
VerDate Mar<15>2010
15:21 Apr 22, 2011
Jkt 223001
John Howard,
Director, National Institute for Occupational
Safety and Health.
[FR Doc. 2011–9928 Filed 4–22–11; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Request for Information (RFI) To
Identify and Obtain Relevant
Information From Public or Private
Entities With an Interest in
Biovigilance
Office of the Assistant
Secretary for Health, Office of the
Secretary, Department of Health and
Human Services.
ACTION: Notice.
AGENCY:
This Request for Information
(RFI) seeks to identify and obtain
relevant information regarding the
possible development of a publicprivate partnership (PPP) designed to
facilitate the identification of risks and
strategies to assure safety of the U.S.
supply of blood and blood components,
tissues, cells, and organs. This RFI is
intended to inform the Department of
Health and Human Services (HHS)
regarding stakeholders, mechanisms,
and approaches on issues related to
developing and managing a PPP and
scope of PPP activities. Replies are
invited from (1) public or private
entities with an interest in biovigilance,
and (2) entities with experience and
capabilities managing public-private
partnerships (PPPs) in the biological
sciences and public health domains.
This RFI is for information and planning
purposes only and is not a solicitation
for applications or an obligation on the
part of the U.S. Government to provide
support for any ideas identified in
response to it. Please note that the U.S.
Government will not pay for the
preparation of any information
submitted or for its use of that
information.
All responses must be received
no later than 4 p.m. EDT on June 9, 2011
at the address listed below.
ADDRESSES: All responses should be
e-mailed to Biovigilance@hhs.gov
(attention Dr. Jerry Holmberg). Please
limit responses to 10 pages. Include in
the subject line, the following
information:
• Name of the institution or site.
• Respondent, title, and full contact
information.
DATES:
PO 00000
Frm 00039
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Dr.
Jerry Holmberg, Senior Advisor for
Blood Safety, Office of the Assistant
Secretary for Health, Office of the
Secretary, U.S. Department of Health
and Human Services, 1101 Wootton
Parkway, Tower Building, Suite 250,
Rockville, MD 20852.
SUPPLEMENTARY INFORMATION: In 2009,
the Advisory Committee on Blood
Safety and Availability (ACBSA) within
the Department of Health and Human
Services (HHS), Office of the Assistant
Secretary of Health, reviewed and
discussed a report on the current state
of biovigilance. In that report
(‘‘Biovigilance: Efforts to Bridge a
Critical Gap in Patient Safety and Donor
Health’’ https://www.hhs.gov/ash/
bloodsafety/biovigilance/),
biovigilance was defined as ‘‘a
comprehensive and integrated national
patient safety program to collect,
analyze, and report on the outcomes of
collection and transfusion and/or
transplantation of blood components
and derivatives, tissues, cells, and
organs. This definition does not include
vaccines, allergenic products, and most
recombinant human proteins.’’ Safety
surveillance for plasma derivatives,
while a logical part of biovigilance,
already falls under FDA mandated drug
adverse event reporting and is not
addressed in the current HHS initiative.
Among the recommendations in that
report was for HHS to develop an HHS
action plan to support a national
biovigilance program, integration of
systems within government and private
sectors, and steps to enhance
mechanisms for surveillance.
HHS is continuing its efforts to
develop an action plan to support a
national biovigilance program for blood
and blood components, tissues, cells,
and organs. As part of these efforts, HHS
is exploring the feasibility of a PPP.
HHS believes that a PPP potentially
could serve as an appropriate
mechanism for achieving the broad
goals and mission of biovigilance. A
PPP might provide the American public
with a mechanism for leveraging and
maximizing resources, for collaborating
on research and problem solving, for
creating new opportunities, and for
advancing the Department’s public
health mission as it relates to challenges
associated with disease prevention
(including emerging infectious diseases
or EIDs), adverse events, and process
improvements.
Biovigilance is an area of growing
importance, with a potential role in any
of the following areas:
• Identifying strategies for protecting
recipients and living donor health;
FOR FURTHER INFORMATION CONTACT:
SUMMARY:
Decision To Evaluate a Petition To
Designate a Class of Employees From
Ames Laboratory in Ames, IA, To Be
Included in the Special Exposure
Cohort
ACTION:
be submitted by e-mail to
DCAS@CDC.GOV.
E:\FR\FM\25APN1.SGM
25APN1
Agencies
[Federal Register Volume 76, Number 79 (Monday, April 25, 2011)]
[Notices]
[Page 22900]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-9928]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Decision To Evaluate a Petition To Designate a Class of Employees
From Ames Laboratory in Ames, IA, To Be Included in the Special
Exposure Cohort
AGENCY: National Institute for Occupational Safety and Health (NIOSH),
Department of Health and Human Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: HHS gives notice as required by 42 CFR 83.12(e) of a decision
to evaluate a petition to designate a class of employees from Ames
Laboratory in Ames, Iowa, to be included in the Special Exposure Cohort
under the Energy Employees Occupational Illness Compensation Program
Act of 2000. The initial proposed definition for the class being
evaluated, subject to revision as warranted by the evaluation, is as
follows:
Facility: Ames Laboratory.
Location: Ames, Iowa.
Job Titles and/or Job Duties: All Department of Energy (DOE)
employees, its predecessor agencies, and its contractors and
subcontractors who worked in any area of the DOE facility.
Period of Employment: January 1, 1942 through December 31, 1970.
FOR FURTHER INFORMATION CONTACT: Stuart L. Hinnefeld, Director,
Division of Compensation Analysis and Support, National Institute for
Occupational Safety and Health (NIOSH), 4676 Columbia Parkway, MS C-46,
Cincinnati, OH 45226, Telephone 877-222-7570. Information requests can
also be submitted by e-mail to DCAS@CDC.GOV.
John Howard,
Director, National Institute for Occupational Safety and Health.
[FR Doc. 2011-9928 Filed 4-22-11; 8:45 am]
BILLING CODE 4163-19-P