Course offering number:0910-709
Course ID:
2339
Implementing and Managing the Medical Device Complaint System
Pre-recorded Course
AN ON-DEMAND ONLINE TRAINING FORMAT
William G. Marshall, President of William G. Marshall and Associates; Consultant to the worldwide drug and device industry as well as to the FDA and worldwide lecturer in GMP related issues.
William G. Marshall is President of William G. Marshall and Associates. He has over twenty years experience in the Pharmaceutical and Medical
Device Manufacturing Environment. Mr. Marshall has held Director level and Chief Operating Officer positions with large multinational
pharmaceutical corporations as well as start-up ventures. He has been the Director of a major reference laboratory, and has been active in clean
room design and validation. In the last five years, he has acted as a third party in several consent decrees.
Mr. Marshall is currently a consultant to the worldwide drug and device industry as well as to the FDA. He lectures worldwide in GMP related
issues including Clean Room Technology and Sterilization. In the past 18 months, he has been involved in 10 Pre-Approval Inspections that
include the first aseptic processed injectables from India, the first ever drugs from Turkey, and APIs from China, that were all approved for
introduction to the US market. He has a Master's Degree in Biology from Georgetown University, Washington, DC.
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