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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:
- Describe current regulations surrounding mHealth and virtual trial apps
- Identify potential IRB considerations for studies involving virtual trial technologies
- Outline ways researchers can prepare protocols for IRB review
Presented By

James Riddle
MCSE, CIP, CPIA, CRQM
VP, Institutional Services
Advarra

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

James Wurdeman
Chief Product Officer, Forte Products
Advarra

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