Clinical trial Essential Documents and managing Trial Files

An interactive course focusing on in-depth 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, and the discussion of typical issues and audit findings along with practical exercises.

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