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.
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Identificador: 44323342
Precio: EUR 309.00 EUR 250.00 (IVA no incluido)
Créditos de servicio:
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