Mitchell Parrish JD, RAC, CIP

Vice President Legal & Regulatory Affairs, Kinetiq

Mitchell Parrish’s practice focuses on FDA law and on issues impacting the research and development of innovative life sciences and digital health products. He provides regulatory, compliance, and transactional services to Quorum Review and to leading manufacturers, IT companies, hospital systems, academic medical centers, and independent researchers.

Mr. Parrish’s experience includes both in-house and outside counsel roles serving as a consultant to the National Cancer Institute, regulatory counsel to Western IRB, and associate attorney at the global law firm K&L Gates. Mr. Parrish is a member of the Washington and Oregon State bars and is a member of the Regulatory Professionals Society. He is a Certified IRB Professional (CIP) and has his Regulatory Affairs Certification (RAC).

Mr. Parrish is a frequent speaker on clinical trial topics and is a published author, including having chapters on prescription drug labeling & promotion and on laws & regulations pertaining to pediatric populations in the most recent edition of the Fundamentals of US Regulatory Affairs text book.


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