Using Electronic Consent and Technologies in Research: Regulatory and IRB Considerations

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Electronic technologies are being viewed as an increasingly popular and effective tool in all aspects of human subject research. In this webinar, Mitchell E. Parrish, JD, RAC, CIP, discusses the regulatory and IRB considerations of using electronic consent and technologies in clinical research.

About the Webinar

Presented by Mitchell E. Parrish, JD, RAC, CIP, the webinar covered:

  • Electronic Consent
  • Electronic Technologies To Facilitate Consent
  • Electronic Data Storage
  • Electronic Data Monitoring

About the Speaker

0232_Mitchell Parrish_2_croppedMitchell Parrish, is the Vice President of Legal Affairs and General Counsel for Kinetiq, a consulting and technology division of Quorum Review IRB.

Mitchell has served in both in-house and outside counsel roles as a consultant to the National Cancer Institute, as a regulatory counsel to a large central IRB, and as an associate attorney at the global law firm K&L Gates. He is a frequent speaker and published author on clinical trials topics.

He is a member of the Washington and Oregon State bars and Regulatory Affairs Professionals Society; is a Certified IRB Professional (CIP); and has his Regulatory Affairs Certification (RAC).

This webinar is eligible for continuing education credits.

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Continuing Education Credits
This webinar is pre-approved for 1.0 contact hours of continuing education credit for the Certified IRB Professional (CIP) certification, and for Maintenance of ACRP’s CCRC®, CCRA®, CCTI® or CPI® certifications. If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements. Information for CE credits for SOCRA can be found here. Visit our Webinars Help page for more information on certification credits.

Certificate of Attendance
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