Clinical trial Essential Documents

An interactive course focusing on the review of the main principles and international requirements for collection, handling and effective management of clinical trial essential documents, and the responsibilities of all the parties involved, including practical exercises

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