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Workshop Focuses on FDA Process

By Amanda White

 

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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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