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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. | 