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By
Amanda
White
Topics
include FDA guidelines for the regulation of reproductive
tissues, cells and products, documentation and record
keeping guidelines, FDA requirements for donor suitability,
and Health Insurance Portability and Accountability
Act guidelines and their impact on ART laboratories.
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Lexington,
Ky. (Nov. 8, 2002) -- The
University of Kentucky College of Health Sciences
and College of Medicine are sponsoring "Developing
a Compliant Practice: The FDA comes to ART."
The workshop will be held from 5 to 7:30 p.m. Friday,
Nov. 8, at the Hilary J. Boone Center and from 9 a.m.
to 5 p.m. Saturday, Nov. 9, at the College of Health
Sciences commons area. The workshop is designed to
introduce the Food and Drug Administration and FDA
regulations to clinicians and scientists in Assisted
Reproductive Technology (ART) laboratories.
Topics
include FDA guidelines for the regulation of reproductive
tissues, cells and products, documentation and record
keeping guidelines, FDA requirements for donor suitability,
and Health Insurance Portability and Accountability
Act guidelines and their impact on ART laboratories.
For more
information, call (859) 257-5320.
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