Events
Adverse Event Reporting During Medical Device Clinical Evaluations
08 December 2009The Rembrandt Hotel
London, UK
Website: www.management-forum.co.uk
This conference aims to help delegates to understand the significance of the revision of the MDD in relation to Adverse Incident Reporting. It will help them gain an overview of the current system in Europe, know the role of the Data Safety Monitoring Board, understand the definitions and classification of adverse events and learn what happens after CE marking.
