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Time is running out to meet all requirements in MDR and IVDR. The new additional regulatory burden and the need to think and act on how to connect the dots when it comes to documentation and products!

Learn more about the challenges posed by Medical Device and In Vitro Medical Device Regulations. Discover how to manage this additional regulatory complexity by improving product documentation.

Viewing time: 30mins

Recording from Life Sciences PLM Innovation Forum 2021.

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Presented by
Peter Löwendahl
Peter Löwendahl
Senior Advisor Quality and Regulatory Affairs, Hoff & Lowendahl)