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Expert in Medical Device: Design, Development, Manufacturing and Quality AssuranceHe 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 ValidationExpert 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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