New Legal Challenges to the Medical Device Industry

This presentation will address some of the new 'legal' issues that manufacturers will need to deal with under the new regulation, such as advertising/claims regulation, new liability clauses for defective devices, new requirements for authorised representatives, obligations for actors in the supply chain, the new responsible person role in the company, new regime for repacking and parts/components and what will still happen on a national level in implementation of the MDR.

Presented by: 
Erik Vollebregt, Partner, Axon Lawyers, Netherlands