96-11070. NCI Cancer Information Service Community Services Database Survey and Verification; Proposed Collection; Comment Request  

  • [Federal Register Volume 61, Number 87 (Friday, May 3, 1996)]
    [Notices]
    [Pages 19943-19944]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 96-11070]
    
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    National Institutes of Health
    
    
    NCI Cancer Information Service Community Services Database Survey 
    and Verification; Proposed Collection; Comment Request
    
    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, 
    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: NCI Cancer Information Service Community 
    Services Database Survey and Verification. Type of Information 
    Collection Request: New. Form Number: not applicable. Need and Use of 
    Information Collection: The CIS provides the general public, cancer 
    patients, families, health professionals, and others with the latest 
    information on cancer. Essential to fulfilling its role as a referral 
    source for cancer patients and their families is the identification, 
    acquisition, and dissemination of information about hospitals, breast 
    and cervical cancer screening clinics, and cancer pain management 
    programs. This effort involves sending a survey tool or a verification 
    instrument annually to 17,135 respondents. Frequency of Response: 
    Annual. Affected Public: Business or other for-profit, not-for-profit 
    institutions, Federal government, state, local or tribal government. 
    Type of Respondents: Administrators of hospitals, clinics, and cancer 
    screening centers. The annual reporting burden is as follows: Estimated 
    Number of Respondents: 17,135; Estimated Number of Responses per 
    Respondent: 1; Average Burden Hours Per Response: .167; and Estimated 
    Total Annual Burden Hours Requested: 2,862. The annualized cost to 
    respondents is estimated at: $34,339. There are no Capital Costs to 
    report. There are no Operating or Maintenance Costs to report.
    
    [[Page 19944]]
    
    
    
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                                                                                                          Estimated 
                                                                                Estimated     Average       total   
                                                                   Estimated    number of      burden       annual  
                         Type of respondents                       number of    responses    hours per      burden  
                                                                  respondents      per        response      hours   
                                                                                respondent                requested 
    ----------------------------------------------------------------------------------------------------------------
    Administrators..............................................       17,135            1         .167        2,862
        Total...................................................  ...........  ...........  ...........        2,862
    ----------------------------------------------------------------------------------------------------------------
    
    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) 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) 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) Ways to enhance the quality, utility, and 
    clarity of the information to be collected; and (4) Ways to 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: To request more information on the proposed 
    project or to obtain a copy of the data collection plans and 
    instruments, contact Chris Thomsen, Acting Chief, Cancer Information 
    Service, National Cancer Institute, NIH, Building 31, Room 10A16, 9000 
    Rockville Pike, Bethesda, MD 20892, or call non-toll-free number (301) 
    496-5583 ext. 239 or E-mail your request, including your address to: 
    thomsenc@occ.nci.nih.gov
    
    COMMENTS DUE DATE: Comments regarding this information collection are 
    best assured of having their full effect if received on or before July 
    2, 1996.
    
        Dated: April 29, 1996.
    Philip D. Amoruso,
    Associate Director of Extramural Management, NCI.
    [FR Doc. 96-11070 Filed 5-2-96; 8:45 am]
    BILLING CODE 4140-01-M
    
    

Document Information

Effective Date:
7/2/1996
Published:
05/03/1996
Department:
National Institutes of Health
Entry Type:
Notice
Document Number:
96-11070
Dates:
Comments regarding this information collection are best assured of having their full effect if received on or before July 2, 1996.
Pages:
19943-19944 (2 pages)
PDF File:
96-11070.pdf