Speaking Engagement: Clinical Trial Research Conference

eConsent adoption is on the rise, and with that comes a heightened focus on the compliance of eConsent platforms and the protection of data. In his session, VP of Legal Affairs Mitchell Parrish will uncover the security and privacy requirements related to eConsent, as well as other important adoption considerations for sponsors, CROs, research sites, and IRBs.

 

About the Speaker

Mitchell Parrish, JD, RAC, CIP, leads the Kinetiq Legal and Regulatory teams, driving consultation on pressing issues impacting innovative medical research, digital health, and software designed to support clinical trials. Mitchell has held both in-house and outside counsel roles, having served as an associate attorney at the global law firm K&L Gates, consultant to the National Cancer Institute, and regulatory counsel to a global provider of medical research review services. He frequently speaks and writes on FDA regulatory, clinical trial, and IRB topics, including authorship of chapters on prescription drug labeling and on research in pediatric populations in the most recent edition of the Fundamentals of US Regulatory Affairs.

 

About the Conference

The Clinical Trials Research Conference, held by UnityPoint Health, will take place in Des Moines, IA, on October 17, 2017. This particular conference focuses on key facets of conducting a successful clinical trial.