The Medical Device Regulation (MDR) might have been delayed in 2020, but the requirements returned in 2020. Not sure how MDR requirements affect your organization? Need help understanding how to deal with MDR? In our webinar, Michelle Lott, Regulatory Strategist and Founder at lean RAQA, and Peter Argondizzo, Founder at Argo Translation, discussed how you can strategically plan for the implications of MDR.
Some of the topics include:
- Who does the MDR impact?
- What actions do you need to take?
- When does translation need to take place?
- What are the quality requirements for your translation vendor?
- Translation best practices
