Wow! An Online Overview of the EU MDR Course!
by Eoin Philip Kelly | January 22, 2020 | Blog , eLearning , EU MDR , Medical Device Regulatory Affairs , Quality , Regulatory Affairs , |
In partnership with Meddev Solutions UK, we are releasing an Online General Overview of the EU MDR Training Course (2hrs) which will be suitable for anyone working in the Medical Device Industry who is looking for a general overview of the EU MDR.
This online, highly interactive course will cover:
- History of MD Scandals, Purpose & Structure of the EU MDR, Definitions, Medical Devices covered by the EU MDR, Key Changes in the EU MDR & Relationship to ISO 13485:2016, 90/385/EEC and 93/42/EEC
- Overview of articles 5-9, Role of Authorised Representative, Obligations of Importer, Distributor and Person Responsible for regulatory compliance, Application of manufacturing obligations to other stakeholders, and EU declaration and CE Marking, and more!
The standard course fee is €195pp but for a limited time only this course is available for just €145pp with discounts offered for volume licenses of 10+
If you have any questions about the course or would like to discuss volume licensing, we would love to hear from you! We can be reached by phone on (061) 529100 or (01) 2552888 or by email at firstname.lastname@example.org – so get in touch!