Review of the regulatory requirements in Europe for post market surveillance, including a practical approach on how to setup systems adapted to a specific product and complying with the regulations are provided in a half day course session.

Program:
• A review of the regulations and what it means in practice to you and your strategy
• Planning the right post market surveillance process
• Working with the data to ensure long-term market presence
• Competent authority roles and obligations
• How to ensure compliance of manufacturers
• Changes in the new medical device directives to expect

Throughout this interactive senior-level workshop, you will be given practical examples and case studies to discuss.



For information on booking D-TARGET training courses, please contact us.