MDR for Clinical Research in Europe

This is the perfect training solution for investigators and research professionals involved in clinical trials with medical devices in Europe, who need to know what has changed since the MDR is in force.

• 4 hours
• Modular and at your own pace
• 6 modules (The Basics, Scope of MDR, Submitting, Safety Reporting and Modifications, Post-Marketing Follow-Up and Vigilance reporting)
• Knowledge test with 25 questions
• Available in Dutch and English
• Focuses on clinical research in Europe
• Online certificate with a test score of 80 or higher