Safety of Clinical Trial Subjects

An interactive course focusing on the review of guidelines of ICH GCP and ICH E2A and the international requirements for clinical trial subjects safety, and the responsibilities of all the parties involved

This course is a prerequisite for further trainings.

Training type: 
Примеры разработанных Клинических Тренингов/Семинаров для начинающих и имеющих начальный опыт мониторинга клинических исследований (Базовый уровень)
Target audience: 
Training/workshop for investigators, clinical trial assistants, clinical trial coordinators, monitors and clinical research specialists
Duration: 
4/6 hrs