As you should know, the Medical Device Regulation (MDR) will be fully implemented in 2020. To inform you about the fundamentals of lifecycle management under the MDR, we would like to invite you to our one-day training course ‘Essentials of Lifecycle Management under the MDR’, organized in cooperation with MDProject at our headquarters in Bilthoven, the Netherlands, on Monday, 17 December 2018. This training course will address:

• Design Control & Risk Management
• Design of your Clinical Investigation
• Use of your Clinical Data in your CERs
• PMS planning

You can register by sending an e-mail to [email protected]. If you have any questions beforehand, please be encouraged to contact us by phone (+31 30 229 2727) or email ([email protected]). We are looking forward to meeting you in Bilthoven!

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