Chris Thom, MD, RDMS — Associate Professor of Emergency Medicine at the University of Virginia School of Medicine — discusses the key parameters for designing studies in clinical testing.
✅ : Ensuring patients fully understand the trial and provide legal consent.
✅ : Implementing a robust plan to safeguard patient data.
✅ : Establishing clear mechanisms for tracking and reporting adverse events.
✅ : Continuous safety analysis and a thorough risk evaluation.
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