Stephen C. Smith

Director of Regulatory Affairs at GID

Stephen is a medical device Quality Assurance and Regulatory executive with over 29 years in the medical device industry. His experience includes developing and implementing quality systems in all elements of 21 CFR 820 (Medical Device Quality System Regulation), ISO 13485 (CE Medical Device) and 21 CFR 1270/1271 (Human Cellular and Tissue Products). At GID BIO Stephen Stephen will direct regulatory affairs and quality assurance, helping to ensure that all products are high quality and comply with government regulations.


  • Director of Regulatory Affairs

    Current role

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