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Health and Safety
Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course
Online
Engels
Identificatie: 44186263
Cursusoverzicht
Wat u leert
This course will provide participants with an overview of the critical changes in relation to EU In Vitro Diagnostic Regulation, along with the implementation timescales.
Voor wie deze cursus bedoeld is
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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Pakket · 2
Introduction to new EU regulations on Medical and In Vitro Diagnostic devices (Two Courses)
Delegates participating in this course will:Gain an overview of the critical changes with EU MDR and EU IVDR, and their implicationsFind out about implementation timescales and their impact on resourcesDiscover what EU MDR and EU IVDR mean in practice