Fundamentals of EU MDR and IVDR – Level 1
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Topic : Health and Medicine; 0
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Description :
This 2 day seminar will go into the specifics of the European Union Medical Device Regulation (EU MDR) and the In Vitro Diagnostic Device Regulation (IVDR), provide case studies and share lessons learned so your organization can benefit from the mistakes of others. We will review the latest changes to the regulations effective and in force for 2020 and will draw out key developments and key dates with particular emphasis on requirements for US firms shipping materials, parts, and products to the European Union.
Topics: European Union Medical Device Regulation (EU MDR), In Vitro Diagnostic Device Regulation (IVDR), Medical Device Regulation, MDD, MDR, GSPR Annex 1, ISO 13485:2016, Quality Management System
Fundamentals of EU MDR and IVDR – Level 1 to be held in Minneapolis, United States between 30 January 2020 and 31 January 2020. It is organised by Complianceonline. It covers specific areas of Health and Medicine such as 0. Visit the website of the conference for more detailed information or contact the organizer for specific questions.
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