Omschrijving

Delegates participating in this course will:

  • Gain an overview of the critical changes with EU MDR and EU IVDR, and their implications
  • Find out about implementation timescales and their impact on resources
  • Discover what EU MDR and EU IVDR mean in practice

Doelstellingen

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.

Doelgroep

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

Bundelcomponenten

Kies een aanbieding voor elk van de bundelcomponenten en klik hieronder op de knop 'Toevoegen aan winkelwagentje':

Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course

Trainingen

Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course

Introduction to the New EU Medical Device Regulation (MDR) eLearning Course

Trainingen

Introduction to the New EU Medical Device Regulation (MDR) eLearning Course

Informatie

44155509

EUR 300.00 EUR 250.00

Deel

Systeem ondervindt momenteel problemen en we werken aan een oplossing. Als u een fout tegenkomt, kom dan snel terug en probeer het opnieuw.
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