Jane R. Brown

Principal Consultant, CAI

Jane has more than thirty-five years quality and regulatory compliance experience in the pharmaceutical and medical device industries and has performed numerous cGMP audits and Quality System assessments for commercial operations and clinical trial supplies manufacturing and testing. In addition, she has conducted pre-approval inspection assessments and provided guidance and advice on regulatory inspection preparation and management. She has a broad knowledge of global regulatory requirements and an awareness of emerging issues and trends in the regulatory environment.

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