Date: 3th of November 2020
Time: 14:00h -16:00 CET
Costs: € 295,-
Package deal ( 12 sessions) : € 3750.-
* Team Members with Different Roles & Responsibilities? No problem!
We offer flexible options for your company, team, or individual experts. You can send different delegates from your company to the sessions and still qualify for the package.
The Medical Devices Regulation (MDR) is the legislation setting out the requirements that manufacturers must meet in order to market medical devices in the European Union. It affects all manufacturers, importers, distributors and representatives of medical devices within the EU. The MDR, which replaces the Medical Devices Directive (93/42/EEC) and Active Implantable Medical Devices Directive (90/385/EEC).
- CE Mark & The EU
- Role of Notified Bodies, Competent Authorities and Others
- Purpose of the MDR
- Core changes MDD to MDR
Who should attend?
Manufacturers of medical devices, especially: Regulatory Affairs, Clinical Affairs Specialists and Quality Assurance specialists.