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Good Laboratory Practices Course
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Designed to cover the FDA's current Good Laboratory Practice regulations and how they affect the conduct of non-clinical laboratory research, this one-day course introduces cGLP requirements, including the role of the Quality Assurance Unit and Study Director, Personnel and Test Facility Organization, Test and Control Articles, cGLP documentation, Study Implementation, and Archiving of Records and Materials.

10/31/2014
When: 10/31/2014
9:00 AM - 4:00 PM
Where: Biotility at UF's Center of Excellence for Regenerative Health Biotechnology
Contact: Tammy Mandell
386-462-6397

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Good Laboratory Practices

Designed to cover the FDA's current Good Laboratory Practice regulations and how they affect the conduct of non-clinical laboratory research, this one-day course introduces cGLP requirements, including the role of the Quality Assurance Unit and Study Director, Personnel and Test Facility Organization, Test and Control Articles, cGLP documentation, Study Implementation, and Archiving of Records and Materials. Hands-on activities include equipment calibration using NIST-traceable reference standards, and in-vitro toxicity testing. REGISTER

DATE: October 31, 2014

PRICE: $350

TIME: 9:00 a.m. - 4:00 p.m.

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