Source Documents and Source Documents Verification

An interactive course focusing on the review of the main principles, standards and international requirements for source documents at investigational sites with practical exercises covering the responsibilities of clinical monitors on the source documents verification and review process.

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 coordinators, monitors and clinical research specialists.
Duration: 
4/6 hrs