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This webinar provides an overview of the current state of the FDA’s Expanded Access Program and state and federal “Right to Try” legislative efforts.
Anthony Keyes reviews the federal regulations regarding registration and results reporting of clinical trials.
Robert Neff and Michele Russell-Einhorn discuss considerations and issues research professionals should be aware of when developing research projects that involve mobile apps.
Emily Chi Fogler and Andrew Rusczek, attorneys practicing at Verrill Dana, LLP, discuss common legal issues for institutions and companies participating in international research.