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Quorum Review’s Mitchell Parrish Presents at Embracing Change: Clinical Research in the 21st Century
Date:9/12/2013

Seattle, WA (PRWEB) September 12, 2013

Quorum Review IRB, the industry leader in central IRB services, announces Mitchell E. Parrish, JD, CIP, as a presenter at the event Embracing Change: Clinical Research in the 21st Century. The event takes place September 21, 2013 at Arizona State University in Phoenix, AZ.

Mr. Parrish presents two topics at the event. His first presentation, “Regulatory Implications of Recruiting Clinical Trial Participants through Social Media,” takes place at 8:30 AM. The presentation covers the use of social media in recruiting research participants and provides the tools necessary to ensure compliance with regulations impacting the use of social media. Mr. Parrish also presents “Understanding Safety and Non-Safety Reporting Obligations in Clinical Trials,” which takes place at 3:00 PM. The presentation unravels the regulatory maze impacting the reporting of safety and non-safety information in clinical trials and simplifies required site and sponsor reporting obligations.

Mr. Parrish is a Regulatory Attorney for Quorum Review, where he provides legal counsel on regulatory issues and FDA requirements associated with research and development of medical products. Mr. Parrish is a member of the Regulatory Affairs Professionals Society, Public Responsibility in Medicine & Research, American Association of Corporate Counsel, and Washington State Bar Association. He is also a Certified IRB Professional (CIP) and guest lectures for the Masters of Science Program in Biomedical Regulatory Affairs at the University of Washington. Prior to Quorum, Mr. Parrish served as Regulatory Counsel for Western IRB and as a Regulatory Consultant for the National Cancer Inst
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