On-Demand Webinar

Accelerating the Recovery – IRB Review of Virtual Trial Technology

As the research community evolves to address the new normal, sponsors and investigators are rushing to incorporate mobile medical applications and other virtual trial technologies into their research. Is your IRB prepared to review protocols involving mHealth and virtual trial apps? What questions should you ask the sponsor or researcher about these technologies? How can researchers at your institution better plan their protocols and documentation to aide IRB review?

If these questions are being asked at your research organization, join James Riddle, Advarra Vice President of Institutional Services, as he explores the current regulatory landscape governing mHealth and virtual trial applications. The webinar also offers practical tips on how IRBs should approach review of research involving these virtual modalities.

Learning Objectives:

  1. Describe current regulations surrounding mHealth and virtual trial apps
  2. Identify potential IRB considerations for studies involving virtual trial technologies
  3. Outline ways researchers can prepare protocols for IRB review

Presented By

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James Riddle


VP, Institutional Services

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Alison Lakin

Associate Vice Chancellor for Regulatory Compliance, and Research Integrity Officer
University of Colorado Denver, Anschutz Medical Campus

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James Wurdeman

Chief Product Officer, Forte Products

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Who should watch?

IRB professionals, sponsors, researchers, and others who seek a better understanding of mobile medical applications

CE Credits

Attendance at this session has been approved for 1.00 contact hour of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations.

This session meets the Certified IRB Professional (CIP) recertification guidelines for a maximum of 1 credit.

The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit. 

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.

Certificate of Attendance

After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.

DATE: July 8, 2020
Time: 1 pm ET | 10 am PT
Duration: 1 hour

Register Now