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Expert in Medical Device: Design, Development, Manufacturing and Quality Assurance
He has been involved in Good Manufacturing Practices (GMP) for over twenty seven years in Class II and III product environment. Set up and maintained Class 100,000 clean rooms and manufactured Class II Critical and Class III devices in this environment. See full profile

New York (NY), USA

Expert in Medical Device Design Control and Software Validation
Expert has extensive medical device engineering development and regulatory experience. He is a certified Lloyds of London ISO 9000 Lead Auditor and a member of the Westlaw Roundtable Expert Witness Network. His regulatory experience is primarily in product ... See full profile

New Jersey (NJ), USA


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