96-31415. Proposed Data Collections Submitted for Public Comment and Recommendations  

  • [Federal Register Volume 61, Number 239 (Wednesday, December 11, 1996)]
    [Notices]
    [Pages 65226-65227]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 96-31415]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Centers for Disease Control and Prevention
    [INFO-97-30]
    
    
    Proposed Data Collections Submitted for Public Comment and 
    Recommendations
    
        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 Centers for Disease Control and 
    Prevention (CDC) will publish periodic summaries of proposed projects. 
    To request more information on the proposed projects or to obtain a 
    copy of the data collection plans and instruments, call the CDC Reports 
    Clearance Officer on (404) 639-7090.
        Comments are invited on: (a) Whether the proposed collection of 
    information is necessary for the proper performance of the functions of 
    the agency, including whether the information shall have practical 
    utility; (b) the accuracy of the agency's estimate of the burden of the 
    proposed collection of information; (c) ways to enhance the quality, 
    utility, and clarity of the information to be collected; and (d) ways 
    to minimize the burden of the collection of information on respondents, 
    including through the use of automated collection techniques for other 
    forms of information technology. Send comments to Wilma Johnson, CDC 
    Reports Clearance Officer, 1600 Clifton Road, MS-D24, Atlanta, GA 
    30333. Written comments should be received within 60 days of this 
    notice.
    
    Proposed Projects
    
        1. Congenital Syphilis Case Investigation and Report Form (CDC 
    73.126 REV 09-91) (0920-0128)--This request is for a 3-year extension 
    of clearance. Reducing congenital syphilis (CS) is a national objective 
    in the DHHS Report entitled Healthy People 2000: Midcourse Review and 
    1995 Revisions. Objective 19.4 of this document states the goal: 
    ``reduce congenital syphilis to an incidence of no more than 40 cases 
    per 100,000 live births'' by the year 2000. In order to meet this 
    national objective, an effective surveillance system for CS must be 
    continued in order to monitor current levels of disease and progress 
    towards the year 2000 objective. This data will also be used to develop 
    intervention strategies and to evaluate ongoing control efforts. The 
    total estimated cost to respondents is $14,550.
    
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                                                                                     Number of   Average            
                                                                        Number of   responses/   burden/     Total  
                               Respondents                             respondents  respondent   response    burden 
                                                                                     (in hrs.)  (in hrs.)  (in hrs.)
    ----------------------------------------------------------------------------------------------------------------
    State and local health department................................        2000            1       0.25        500
                                                                                                          ----------
          Total......................................................  ...........  ..........  .........        500
    ----------------------------------------------------------------------------------------------------------------
    
        2. Survey to Evaluate the 1989 Revisions of the U.S. Standard 
    Certificates of Live Birth and Death and the U.S. Standard Report of 
    Fetal Death--New--OMB approved the information collections for the 
    evaluation of the 1978 revisions of the U.S. standard certificates and 
    reports under OMB No. 0937-0114. The standard certificates are used by 
    state vital statistics offices as models in developing their own birth, 
    death, and fetal death reporting forms. Data obtained from these 
    reporting forms in each individual state are used to compile national 
    vital statistics. The standard certificates are the principal means of 
    achieving uniformity of information upon which national vital 
    statistics are based. To ensure that the standard certificates meet the 
    various
    
    [[Page 65227]]
    
    needs for which they are designed, it is essential that they be 
    evaluated and revised periodically. This information collection will be 
    used to evaluate the items on the 1989 revisions of the standard 
    certificates and to determine if there is other information that should 
    be included on the standards that is needed for relevant public health 
    research. Respondents will include individuals and organizations who 
    are involved in the completion of vital records or who utilize vital 
    statistics data and have an interest in the content of the standard 
    certificates. The information collected will be used by a group of 
    consultants to determine what changes may be needed in the 1989 
    standard certificates. The total cost to respondents is estimated at 
    $90,000.
    
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                                                                                                 Average            
                                                                      Number of     Number of    burden/     Total  
                              Respondents                            respondents  respondents/   response    burden 
                                                                                    responses   (in hrs.)  (in hrs.)
    ----------------------------------------------------------------------------------------------------------------
    Live Birth Questionnaire.......................................        2000             1         0.5       1000
    Fetal Death Questionnaire......................................        2000             1         0.5       1000
    Death Questionnaire............................................        2000             1         0.5       1000
                                                                                                          ----------
          Total....................................................  ...........  ............  .........       3000
    ----------------------------------------------------------------------------------------------------------------
    
        Dated: December 4, 1996.
    Wilma G. Johnson,
    Acting Associate Director for Policy Planning and Evaluation, Centers 
    for Disease Control and Prevention (CDC).
    [FR Doc. 96-31415 Filed 12-10-96; 8:45 am]
    BILLING CODE 4163-18-P
    
    
    

Document Information

Published:
12/11/1996
Department:
Centers for Disease Control and Prevention
Entry Type:
Notice
Document Number:
96-31415
Pages:
65226-65227 (2 pages)
Docket Numbers:
INFO-97-30
PDF File:
96-31415.pdf