[Federal Register Volume 63, Number 129 (Tuesday, July 7, 1998)]
[Notices]
[Pages 36698-36699]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 98-17917]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention


Clinical Laboratory Improvement Advisory Committee (CLIAC): 
Meeting

    Name: CLIAC, Workgroup on Genetic Testing.
    Times and Dates: 8:30 a.m.-5 p.m., July 30, 1998; 8:30 a.m.-5 
p.m., July 31, 1998.

[[Page 36699]]

    Place: CDC, Koger Center, Williams Building, Conference Rooms 
1802 and 1805, 2877 Brandywine Road, Atlanta, Georgia 30341.
    Status: Open to the public, limited only by the space available. 
The meeting rooms accommodate approximately 85 people.
    Purpose: This workgroup advises CLIAC on issues related to 
Genetic Testing.
    Matters to be Discussed: The workgroup will discuss and revise 
recommendations for general or specific Clinical Laboratory 
Improvement Amendments (CLIA) requirements for pre-analytic, 
analytic, and post-analytic components of genetic testing.
    Agenda items are subject to change as priorities dictate.
    Contact Person for Additional Information: John C. Ridderhof, 
Dr. P.H., Division of Laboratory Systems, Public Health Practice 
Program Office, CDC, 4770 Buford Highway, NW Mailstop G-25, Atlanta, 
Georgia 30341, telephone 770/488-8076, FAX 770/488-8282.

    Dated: June 26, 1998.
Carolyn J. Russell,
Director, Management Analysis and Services Office, Centers for Disease 
Control and Prevention (CDC).
[FR Doc. 98-17917 Filed 7-6-98; 8:45 am]
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