1999 - 2008 Senior Director, Product Development, Preclinical and Regulatory Affairs @ NexMed (U.S.A.), Inc.
1998 - 1999 Director Product Development and Project Management @ Lavipharm Laboratories
1992 - 1998 Director Regulatory Affairs and Quality Assurance, Project Management and Transdermal Development @ PharMetrix Division of TCPI (formerly Division of PharmaPatch PLC and PharMetrix
1983 - 1992 Senior Scientist, Manager Controlled Release laboratory @ Dow Corning Corp., Medical Materials Business
William Pfister Education
Purdue University
Ph.D. (Pharmacology & Toxicology)
1976 - 1978
Purdue University
Master of Science (M.S.) (Pharmacology & Toxicology)
1974 - 1976
University of New Hampshire
Bachelor of Science (B.S.) (Biochemistry)
1971 - 1973
William Pfister Skills
Directory Pharmaceutical Regulatory Affairs
Pharmaceutical Management Executive - Global Regulatory Strategies
Regulatory Affairs
Regulatory Submissions (INDs, ANDAs, NDAs, eCTDs)
Regulatory Compliance (GLPs, GCPs, GMPs, ISO)
Product Development
Transdermal and Topical Product Development
Intraoral Drug Delivery Systems
Chemistry Manufacturing Controls (CMC)
Program - Project Management
William Pfister Summary
William Pfister, based in Trenton, NJ, US, is currently a Senior Director Development Regulatory Affairs at Acorda Therapeutics, Inc.. William Pfister brings experience from previous roles at Pfister Consulting, Aprecia Pharmaceuticals Company, Burke Pharmaceutical Research, Inc. and Sonar Products, Inc.. William Pfister holds a 1976 - 1978 Ph.D. in Pharmacology & Toxicology @ Purdue University. With a robust skill set that includes Directory Pharmaceutical Regulatory Affairs, Pharmaceutical Management Executive - Global Regulatory Strategies, Regulatory Affairs, Regulatory Submissions (INDs, ANDAs, NDAs, eCTDs), Regulatory Compliance (GLPs, GCPs, GMPs, ISO) and more. William Pfister has 1 emails and 3 mobile phone numbers on RocketReach.
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