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Monday, Dec 17, 2018

Essentials on Lifecycle Management under the EU MDR

Description

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 trainingen@mdproject.nl. If you have any questions beforehand, please be encouraged to contact us by phone (+31 30 229 2727) or email (bd@factory-cro.com). We are looking forward to meeting you in Bilthoven!

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Date & Time
Monday, Dec 17, 2018
All day

Monday, Dec 17, 2018 Monday, Dec 17, 2018 Europe/London Essentials on Lifecycle Management under the EU MDR Factory CRO for Medical Devices B.V., Professor Bronkhorstlaan, Bilthoven, Nederland
Location
Factory CRO for Medical Devices B.V., Professor Bronkhorstlaan, Bilthoven, Nederland
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