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Shive is responsible for formulation and process development of clients� products, including meeting clients� needs for elegant, effective dosage forms using processes that exceed the U.S. Food and Drug Administration�s current Good Manufacturing Practices (cGMP) requirements. Shive has extensive experience in writing and editing regulatory documents for filing with the FDA to obtain approval for clients� new pharmaceutical products. Shive holds a bachelor�s of science degree in pharmacy from the University of Georgia and a bachelor�s of science degree in textiles from Clemson University in South Carolina. | 