Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Current Good Manufacturing Practices and Related Regulations for Blood and Blood Components; and Requirements for Donor Testing, Donor Notification, and “Lookback”, 123 [E5-8134]

Download as PDF 123 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 Activities; Announcement of Office of Management and Budget Approval; 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 Act of 1995. FOR FURTHER INFORMATION CONTACT: Jonna Capezzuto, Office of Management Programs (HFA–250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301–827–4659. 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 displays a currently valid OMB control number. OMB has now approved the information collection and has assigned VerDate Mar<15>2010 15:46 Nov 10, 2010 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: E5-8134]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 2005N-0220]


Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approval; 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.

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 Act of 1995.

FOR FURTHER INFORMATION CONTACT: Jonna Capezzuto, Office of Management 
Programs (HFA-250), Food and Drug Administration, 5600 Fishers Lane, 
Rockville, MD 20857, 301-827-4659.

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 displays 
a currently valid OMB control number. OMB has now approved the 
information collection and has assigned 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.

    Dated: December 22, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E5-8134 Filed 12-30-05; 8:45 am]
BILLING CODE 4160-01-S
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