Delegates participating in this course will:
About the EU MDR and EU IVDR
The EU MDR and EU IVDR were published in the Official Journal of the European Union on May 5, 2017 as Regulation (EU) 2017/745 and Regulation EU (2017/746). The new rules will apply after a transition period of three years for MDR and five years for IVDR. These two eLearning courses will help medical device and In Vitro diagnostic device manufacturers understand the complex new regulations.
This course is intended for, but not limited to, regulatory personnel, managers, CEO, CFO, or any medical device or IVD field personnel who want to learn about the new regulations.
Choose an offering for each one of the bundle components then click on 'Add To Cart' button below:
There are no Offerings available for this course.
Identifier: 44323042
Price: CLP 224420 CLP 192444
Service Credits:
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