Descripción

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

Objetivos

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.

Audiencia

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.


Componentes del paquete

Elija una oferta para cada uno de los componentes del paquete y luego haga clic en el botón 'Agregar al carrito' a continuación:

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

Modalidades

No hay Modalidades disponibles para este curso

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

Modalidades

No hay Modalidades disponibles para este curso

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CLP 224420 CLP 192444

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