Proposed Collection; Comment Request; Follow-Up of Kidney Cancer Patients From the Central European Multicenter Case-Control Study, 65387-65388 [E8-26086]

Download as PDF sroberts on PROD1PC70 with NOTICES Federal Register / Vol. 73, No. 213 / Monday, November 3, 2008 / Notices of the Food and Drug Administration (FDA). At least one portion of the meeting will be closed to the public. Name of Committee: Vaccines and Related Biological Products Advisory Committee. General Function of the Committee: To provide advice and recommendations to the agency on FDA’s regulatory issues. Date and Time: The meeting will be held on November 20, 2008, from 1 p.m. to approximately 4 p.m. Location: National Institutes of Health, Building 29B, Conference Room C. This meeting will be held by teleconference. The public is welcome to attend the meeting at the specified location where a speakerphone will be provided. Public participation in the meeting is limited to the use of the speakerphone in the conference room. 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Please visit our Web site at https://www.fda.gov/oc/advisory/ default.htm for procedures on public conduct during advisory committee meetings. Dated: October 21, 2008. Randall W. Lutter, Deputy Commissioner for Policy. [FR Doc. E8–26139 Filed 10–31–08; 8:45 am] BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Proposed Collection; Comment Request; Follow-Up of Kidney Cancer Patients From the Central European Multicenter Case-Control Study SUMMARY: In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the National Cancer Institute (NCI), the National Institutes of Health (NIH) will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval. Proposed Collection: Title: Follow-up of Kidney Cancer Patients from the Central European Multicenter CaseControl Study. Type of Information Collection Request: New. Need and Use of Information Collection: The purpose of this questionnaire is to obtain information on the 5-year survival status of kidney cancer patients that were enrolled in a Central European CaseControl Study of Kidney Cancer that was conducted between 2001–2004. The aim is to assess survival, the prevalence of recurrent disease and progression, and to investigate patient, tumor and genetic determinants of survival among cases. The questionnaire will collect information on patient related factors, tumor related factors not collected during the initial study, and the type of treatment(s) received since the patients were last contacted for the case-control study. This questionnaire adheres to The Public Health Service Act, section 412 (42 U.S.C. 285a–1) and section 413 (42 U.S.C. 285a–2), which authorizes the Division of Cancer Epidemiology and Genetics of the National Cancer Institute (NCI) to establish and support programs for the detection, diagnosis, prevention and treatment of cancer; and to collect, identify, analyze and disseminate information on cancer research, diagnosis, prevention and E:\FR\FM\03NON1.SGM 03NON1 65388 Federal Register / Vol. 73, No. 213 / Monday, November 3, 2008 / Notices treatment. Frequency of Response: Once. Affected Public: Individuals. Type of Respondents: Individuals that had previously participated in the Central European Renal Cancer Case-Control Study between 2001–2004 and physician abstractors. The estimated total annual burden hours requested is 296. The annualized cost to respondents is estimated at $5174. There are no additional capital costs, operating costs, and/or maintenance costs to report. TABLE 1—ESTIMATES OF ANNUAL BURDEN HOURS Average time per response (minutes/ hour) Annual burden hours Number of respondents Frequency of response Patients ............................................................................................................................ Families (NOK) ................................................................................................................ Physicians ........................................................................................................................ 200 240 10 1 1 1 40/60 40/60 15/60 133.33 160.00 2.50 Totals ........................................................................................................................ 450 .................... .................... 295.83 Type of respondents Request for Comments: Written comments and/or suggestions from the public and affected agencies are invited on one or more of the following points: (1) Evaluate whether the proposed collection of information is necessary for the proper performance of the function of the agency, including whether the information will have practical utility; (2) Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (3) Enhance the quality, utility, and clarity of the information to be collected; and (4) Minimize the burden of the collection of information on those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology. To request more information on the proposed project or to obtain a copy of the data collection plans and instruments, contact Lee E. Moore, PhD, MPH, Investigator/Epidemiologist, Occupational and Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Executive Plaza South, Room 8102, 6120 Executive Blvd., EPS–MSC 7240, Bethesda, MD 20892–7270 or call nontoll-free number 301–496–6427 or email your request, including your address to: moorele@mail.nih.gov. Comments Due Date: Comments regarding this information collection are best assured of having their full effect if received within 60 days of the date of this publication. sroberts on PROD1PC70 with NOTICES FOR FURTHER INFORMATION CONTACT: VerDate Aug<31>2005 16:58 Oct 31, 2008 Jkt 217001 Dated: October 24, 2008. Vivian Horovitch-Kelley, NCI Project Clearance Liaison Office, National Institutes of Health. [FR Doc. E8–26086 Filed 10–31–08; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Center for Scientific Review; Notice of Closed Meetings Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. Appendix 2), notice is hereby given of the following meetings. The meetings will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. 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. Name of Committee: Center for Scientific Review Special Emphasis Panel; Review of KNOD and NAME Member Conflicts. Date: November 20, 2008. Time: 9 a.m. to 12 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892 (Telephone Conference Call). Contact Person: Elisabeth Koss, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 3152, MSC 7770, Bethesda, MD 20892, (301) 435– 1721, kosse@csr.nih.gov. This notice is being published less than 15 days prior to the meeting due to the timing PO 00000 Frm 00105 Fmt 4703 Sfmt 4703 limitations imposed by the review and funding cycle. Name of Committee: Center for Scientific Review Special Emphasis Panel Shared Instrumentation. Date: November 20–21, 2008. Time: 8 p.m. to 5 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892 (Virtual Meeting). Contact Person: David Balasundaram, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 5189, MSC 7840, Bethesda, MD 20892, 301–435– 1022, balasundaramd@csr.nih.gov. This notice is being published less than 15 days prior to the meeting due to the timing limitations imposed by the review and funding cycle. Name of Committee: AIDS and Related Research Integrated Review Group AIDS Molecular and Cellular Biology Study Section. Date: November 24, 2008. Time: 8 a.m. to 6 p.m. Agenda: To review and evaluate grant applications. Place: The Fairmont Hotel, 2401 M Street, NW., Washington, DC 20037. Contact Person: Kenneth A. Roebuck, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 5214, MSC 7852, Bethesda, MD 20892, (301) 435– 1166, roebuckk@csr.nih.gov. Name of Committee: Center for Scientific Review Special Emphasis Panel Aging Program Project Review. Date: November 24–25, 2008. Time: 8 a.m. to 8 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 6701 Rockledge Drive,, Bethesda, MD 20892 (Virtual Meeting). Contact Person: Seetha Bhagavan, PhD, Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 1126, MSC 7846, Bethesda, MD 20892, (301) 435– 1121, bhagavas@csr.nih.gov. E:\FR\FM\03NON1.SGM 03NON1

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[Federal Register Volume 73, Number 213 (Monday, November 3, 2008)]
[Notices]
[Pages 65387-65388]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-26086]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Proposed Collection; Comment Request; Follow-Up of Kidney Cancer 
Patients From the Central European Multicenter Case-Control Study

SUMMARY: In compliance with the requirement of section 3506(c)(2)(A) of 
the Paperwork Reduction Act of 1995, for opportunity for public comment 
on proposed data collection projects, the National Cancer Institute 
(NCI), the National Institutes of Health (NIH) will publish periodic 
summaries of proposed projects to be submitted to the Office of 
Management and Budget (OMB) for review and approval.
    Proposed Collection: Title: Follow-up of Kidney Cancer Patients 
from the Central European Multicenter Case-Control Study. Type of 
Information Collection Request: New. Need and Use of Information 
Collection: The purpose of this questionnaire is to obtain information 
on the 5-year survival status of kidney cancer patients that were 
enrolled in a Central European Case-Control Study of Kidney Cancer that 
was conducted between 2001-2004. The aim is to assess survival, the 
prevalence of recurrent disease and progression, and to investigate 
patient, tumor and genetic determinants of survival among cases. The 
questionnaire will collect information on patient related factors, 
tumor related factors not collected during the initial study, and the 
type of treatment(s) received since the patients were last contacted 
for the case-control study. This questionnaire adheres to The Public 
Health Service Act, section 412 (42 U.S.C. 285a-1) and section 413 (42 
U.S.C. 285a-2), which authorizes the Division of Cancer Epidemiology 
and Genetics of the National Cancer Institute (NCI) to establish and 
support programs for the detection, diagnosis, prevention and treatment 
of cancer; and to collect, identify, analyze and disseminate 
information on cancer research, diagnosis, prevention and

[[Page 65388]]

treatment. Frequency of Response: Once. Affected Public: Individuals. 
Type of Respondents: Individuals that had previously participated in 
the Central European Renal Cancer Case-Control Study between 2001-2004 
and physician abstractors. The estimated total annual burden hours 
requested is 296. The annualized cost to respondents is estimated at 
$5174. There are no additional capital costs, operating costs, and/or 
maintenance costs to report.

                                    Table 1--Estimates of Annual Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                          Average
                                                                                          time per      Annual
                     Type of respondents                       Number of    Frequency     response      burden
                                                              respondents  of response   (minutes/      hours
                                                                                           hour)
----------------------------------------------------------------------------------------------------------------
Patients....................................................          200            1        40/60       133.33
Families (NOK)..............................................          240            1        40/60       160.00
Physicians..................................................           10            1        15/60         2.50
                                                             ---------------------------------------------------
    Totals..................................................          450  ...........  ...........       295.83
----------------------------------------------------------------------------------------------------------------

    Request for Comments: Written comments and/or suggestions from the 
public and affected agencies are invited on one or more of the 
following points: (1) Evaluate whether the proposed collection of 
information is necessary for the proper performance of the function of 
the agency, including whether the information will have practical 
utility; (2) Evaluate the accuracy of the agency's estimate of the 
burden of the proposed collection of information, including the 
validity of the methodology and assumptions used; (3) Enhance the 
quality, utility, and clarity of the information to be collected; and 
(4) Minimize the burden of the collection of information on those who 
are to respond, including the use of appropriate automated, electronic, 
mechanical, or other technological collection techniques or other forms 
of information technology.

FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the data collection plans and 
instruments, contact Lee E. Moore, PhD, MPH, Investigator/
Epidemiologist, Occupational and Environmental Epidemiology Branch, 
Division of Cancer Epidemiology and Genetics, National Cancer 
Institute, NIH, DHHS, Executive Plaza South, Room 8102, 6120 Executive 
Blvd., EPS-MSC 7240, Bethesda, MD 20892-7270 or call non-toll-free 
number 301-496-6427 or e-mail your request, including your address to: 
moorele@mail.nih.gov.
    Comments Due Date: Comments regarding this information collection 
are best assured of having their full effect if received within 60 days 
of the date of this publication.

    Dated: October 24, 2008.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison Office, National Institutes of Health.
[FR Doc. E8-26086 Filed 10-31-08; 8:45 am]
BILLING CODE 4140-01-P
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