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Spotlight Symposia: The Do’s and Don’ts of Compensating Research Participants: Guidance for Clinical Research Stakeholders
Session Chair(s)
WCG IRB
United States
Join our symposia to hear our industry experts:
- Interpret the regulatory guidances from FDA, OHRP and SACHRP on compensation
- Shed light on the different types of compensation and payments clinical trial participants can receive in a study
- Outline how stakeholders can work with their IRB partner to determine optimal compensation and build processes into their clinical trial design
Speaker(s)
David Borasky, MPH
WCG Clinical, United States
Vice President, IRB Compliance
Jennifer Peterson, RAC
Syneos Health, United States
Executive Director, Study Start up & Regulatory - Americas