Quorum Review’s Mitchell Parrish Presenting at DIA 2014 Conference

DIA_2014_QIRBSEATTLE, WA (May 29, 2014): Quorum Review IRB, the industry leader in central IRB services, announces Mitchell E. Parrish, JD, RAC, CIP, as a presenter at DIA’s 50th Annual Meeting. The event takes place June 15-19, 2014 at the San Diego Convention Center in San Diego, California.

Mr. Parrish speaks on the topic of Research Consent in Acute Settings at 10:30 AM on June 17, 2014. The presentation focuses on the inherent obstacles of this type of research, as well as concrete ways to obtain effective consent while concurrently respecting the research participant, study design, and enrollment numbers. Quorum Review’s Business Development Team will also be present in the exhibition hall at Booth #2030 during the conference dates.

Mitchell Parrish ImageMr. Parrish is a Regulatory Attorney for Quorum Review, where he provides legal counsel on U.S. and Canadian laws and regulations related to medical product research and development. Mr. Parrish is a member of the Regulatory Affairs Professionals Society, Public Responsibility in Medicine & Research, Association of Corporate Counsel, and Washington State Bar Association. He also has his Regulatory Affairs Certification (RAC) and is a Certified IRB Professional (CIP). Prior to Quorum, Mr. Parrish served as a Regulatory Consultant to the National Cancer Institute.

DIA’s Annual Meeting is the nation’s largest multidisciplinary event bringing together a community of life sciences professionals at all levels and across all disciplines involved in the discovery, development, and life cycle management of medical products. These professionals share a common goal to foster innovation that will lead to the development of safe and effective medical products and therapies to patients.

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