Safety of Clinical Trial Subjects

An interactive course focusing on the in-depth review of guidelines of ICH GCP and ICH E2A and the international requirements for clinical trial subjects safety, safety reports and the responsibilities of all the parties involved along with practical exercises covering the discussion of the challenging situations related to safety of clinical trial subjects.

Training type: 
Примеры разработанных Клинических Тренингов/Семинаров для имеющих опыт участников клинических исследований/ мониторинга клинических исследований (Профессиональный уровень)
Target audience: 
Training/workshop for experienced monitors and clinical research specialists, investigators, clinical trial assistants, clinical trial coordinators
Duration: 
6/8 hrs