Implementing electronic technologies may facilitate research, improve research efficiency, and benefit research participants. However, successfully implementing these technologies requires understanding the applicable regulatory requirements and IRB considerations. This Webinar will address electronic technologies for obtaining consent, facilitating consent, storing study data, and monitoring study data. For each of these four topics, the presenter will discuss the current regulatory and IRB framework to ensure compliance and a successful IRB submission.
Presented By: Mitchell E. Parrish, JD, CIP
About the Presenter:
Mitchell Parrish joined Quorum Review IRB in January 2010 as a Regulatory Attorney in Quorum Review’s Regulatory Department. Prior to working at Quorum, Mr. Parrish worked as Regulatory Counsel for Western IRB and as a regulatory advisor to the National Cancer Institute’s Central IRB. Mr. Parrish is CIP certified.