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Virtual Clinical Trials
Session Chair(s)
Lucas Garmon
Recruitment Manager, Patient Recruitment Solutions, ICON plc., United States
This session will discuss how virtual clinical trials represent a relatively new method of collecting safety and efficacy data from clinical trial participants, from study start-up through execution to follow-up.
Learning Objective : Discuss the concept of assessing a protocol visit by visit to identify opportunities to minimize patient burden of participation; Discuss how to appraise and choose the right visit location, data collection method, patient support service or technology for each visit; Design and plan trials that consider patient burden enabled by utilizing relevant technology or patient support services.
Speaker(s)
A Patient-Centric Approach to Study Visits and Data Collection: What if I'm not Ready for 100% Virtual Trial?
Recruitment Manager, Patient Recruitment Solutions, ICON plc., United States
Research Passport: Ethics Review and Regulatory Implications for Participants in Virtual Trials
Senior Consulant and Senior Regulatory Attorney, Advarra, United States
Back to the Future with Virtual Clinical Trials
Lead Clinical Data Manager, Merck, Sharp and Dohme, Colombia
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