The aim of this online comprehensive course was to provide the knowledge and train attendees to be able to act as “Person Responsible for Regulatory Compliance” within their organisations under the Medical Device and In-Vitro Diagnostic Regulations (MDR & IVDR).
WHAT WAS IT ALL ABOUT?
- Up-to-date: MDR & IVDR Regulations: Key changes and implementation
- Comprehensive: Comprehend the conformity assessment paths and how they apply
- Relevant: Understand the MDR & IVDR essential requirements
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