David has over 16 years of experience in QMS project management, GxP compliance, and QC analytical benchwork. He has implemented and maintained international regulatory standards such as ISO 9001, ISO 13485, and ISO 17025 for multiple pharmaceutical, biotech, and medical device companies.
At Cision, David developed the company’s QMS system, managed ISO 13485 certification and audits, and FDA registration and submissions.
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