EU Medical Devices Regulation and EU In Vitro Diagnostic Devices Regulation Training Courses
Enhance your knowledge of the new EU Medical Devices Regulation (MDR) and In Vitro Diagnostic Medical Devices Regulation (IVDR) with eLearning courses from SGS. Learn more about the main requirements of these regulations and how they will affect your organisation.
eLearning: an introduction
In a fast-changing world, nothing stays the same for long. Organisations and individuals need to keep up to date with regulations and advances in technology, as well as dynamic global markets.
SGS provides a wide range of eLearning courses that answer these demands. Meeting the needs and expectations of a new generation of technically proficient professionals, our online courses allow you to keep your professional qualifications, industrial expertise and skills up to date while taking advantage of the flexibility they offer.
eLearning provides the opportunity to learn anytime and anywhere, benefiting both employers and employees.
Delegates participating in these training courses will:
- Gain an overview of the critical requirements to 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
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.
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MDR and IVDR
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