Translational Research Working Group Public Comment Period, 123 [05-24687]
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Federal Register / Vol. 71, No. 1 / Tuesday, January 3, 2006 / Notices
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
No. of
Respondents
21 CFR Section
210 and 211
Annual Frequency
per Response
285
Total Annual
Responses
1
Hours per
Response
285
Total Hours
.25
Total
71.25
71.25
1There
are no capital costs or operating and maintenance costs associated with this collection of information.
Dated: December 22, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
OMB control number 0910–0116. The
approval expires on December 31, 2008.
A copy of the supporting statement for
this information collection is available
on the Internet at https://www.fda.gov/
ohrms/dockets.
ADDRESSES: Comments may be
submitted electronically at the TRWG
Web site: https://www.cancer.gov/trwg/.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: December 22, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
Food and Drug Administration
[FR Doc. E5–8134 Filed 12–30–05; 8:45 am]
The National Cancer Institute is
committed to speeding the development
of new diagnostic tests, cancer
treatments, and other interventions that
benefit people with cancer and people
at risk for cancer. Such development
relies on strong translational research
collaborations between basic and
clinical scientists to generate novel
approaches. Currently, NCI supports a
variety of projects that build this bridge
between basic science and patient care.
Over the next year, the Translational
Research Working Group (TRWG) will
review NCI’s current intramural and
extramural translational research
portfolio (within the scope of the TRWG
mission), facilitate broad community
input, invite public comment, and
recommend ways to improve and
integrate efforts. The ultimate goal is to
accelerate progress toward improving
the health of the nation and cancer
patient outcomes.
[FR Doc. E5–8113 Filed 12–30–05; 8:45 am]
BILLING CODE 4160–01–S
BILLING CODE 4160–01–S
[Docket No. 2005N–0220]
Agency Information Collection
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Current Good Manufacturing Practices
and Related Regulations for Blood and
Blood Components; and Requirements
for Donor Testing, Donor Notification,
and ‘‘Lookback’’
AGENCY:
Food and Drug Administration,
HHS.
rmajette on DSK29S0YB1PROD with NOTICES6
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Current Good Manufacturing Practices
and Related Regulations for Blood and
Blood Components; and Requirements
for Donor Testing, Donor Notification,
and ‘Lookback’’’ has been approved by
the Office of Management and Budget
(OMB) under the Paperwork Reduction
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FOR FURTHER INFORMATION CONTACT:
Jonna Capezzuto, Office of Management
Programs (HFA–250), Food and Drug
Administration, 5600 Fishers Lane,
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SUPPLEMENTARY INFORMATION: In the
Federal Register of October 24, 2005 (70
FR 61447), the agency announced that
the proposed information collection had
been submitted to OMB for review and
clearance under 44 U.S.C. 3507. An
agency may not conduct or sponsor, and
a person is not required to respond to,
a collection of information unless it
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information collection and has assigned
VerDate Mar<15>2010
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Jkt 223001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institute of Health
Translational Research Working Group
Public Comment Period
AGENCY: National Cancer Institute (NCI),
National Institutes of Health (NIH),
Department of Health and Human
Services (DHHS).
ACTION: Request for public comment.
SUMMARY: The Translational Research
Working Group (TRWG), a broad panel
including advocates, researchers from
academia, industry representatives, and
government officials, was established in
early 2005 to evaluate the status of the
National Cancer Institute’s (NCI)
intramural and extramural investment
in translational research in order to
develop recommendations on ways to
coordinate and optimally integrate
activities. The TRWG is also charged
with developing implementation
strategies that will enable the scientific
community and NCI leadership to
appropriately prioritize its translational
research opportunities.
Recommendations will be made to the
National Cancer Advisory Board by
early 2007. To assist in its future
planning efforts, TRWG is asking public
stakeholders in the translational
research enterprise for feedback on
some of the key questions facing the
panel and insights on how to proceed.
DATES: The TRWG public comment
period will run from December 20, 2005
to January 20, 2006.
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
Background
Request for Comments
To better understand the different
viewpoints in the cancer research
community, and to develop and reflect
a common understanding about the
challenges and opportunities in
translational research, TRWG seeks
input on six important areas:
• Barriers to/Incentives for
Translational Research.
• Prioritization.
• Funding.
• System Organization.
• Facilities/Technologies.
• Manpower/Training.
Dated: December 22, 2005.
Ernest Hawk,
Director, Office of Centers, Training and
Resources, National Cancer Institute,
National Institutes of Health.
[FR Doc. 05–24687 Filed 12–30–05; 8:45 am]
BILLING CODE 4140–01–M
E:\FR\FM\03JAN1.SGM
03JAN1
]]>Agencies
[Federal Register Volume 71, Number 1 (Tuesday, January 3, 2006)]
[Notices]
[Page 123]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-24687]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institute of Health
Translational Research Working Group Public Comment Period
AGENCY: National Cancer Institute (NCI), National Institutes of Health
(NIH), Department of Health and Human Services (DHHS).
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Translational Research Working Group (TRWG), a broad panel
including advocates, researchers from academia, industry
representatives, and government officials, was established in early
2005 to evaluate the status of the National Cancer Institute's (NCI)
intramural and extramural investment in translational research in order
to develop recommendations on ways to coordinate and optimally
integrate activities. The TRWG is also charged with developing
implementation strategies that will enable the scientific community and
NCI leadership to appropriately prioritize its translational research
opportunities. Recommendations will be made to the National Cancer
Advisory Board by early 2007. To assist in its future planning efforts,
TRWG is asking public stakeholders in the translational research
enterprise for feedback on some of the key questions facing the panel
and insights on how to proceed.
DATES: The TRWG public comment period will run from December 20, 2005
to January 20, 2006.
ADDRESSES: Comments may be submitted electronically at the TRWG Web
site: https://www.cancer.gov/trwg/.
SUPPLEMENTARY INFORMATION:
Background
The National Cancer Institute is committed to speeding the
development of new diagnostic tests, cancer treatments, and other
interventions that benefit people with cancer and people at risk for
cancer. Such development relies on strong translational research
collaborations between basic and clinical scientists to generate novel
approaches. Currently, NCI supports a variety of projects that build
this bridge between basic science and patient care.
Over the next year, the Translational Research Working Group (TRWG)
will review NCI's current intramural and extramural translational
research portfolio (within the scope of the TRWG mission), facilitate
broad community input, invite public comment, and recommend ways to
improve and integrate efforts. The ultimate goal is to accelerate
progress toward improving the health of the nation and cancer patient
outcomes.
Request for Comments
To better understand the different viewpoints in the cancer
research community, and to develop and reflect a common understanding
about the challenges and opportunities in translational research, TRWG
seeks input on six important areas:
Barriers to/Incentives for Translational Research.
Prioritization.
Funding.
System Organization.
Facilities/Technologies.
Manpower/Training.
Dated: December 22, 2005.
Ernest Hawk,
Director, Office of Centers, Training and Resources, National Cancer
Institute, National Institutes of Health.
[FR Doc. 05-24687 Filed 12-30-05; 8:45 am]
BILLING CODE 4140-01-M
