The new Medical Device Regulation (MDR), published in May 2017, replaces the Medical Device Directive (MDD) 93/42/EEC6.
As a medical device manufacturer, you have three years from May 25, 2017 to transition to the MDR. Within this period, manufacturers will need to update their technical documentation and processes in order to meet the requirements of the new regulation.
Lloyd's Register has created an On-Demand webcast to help your organization understand the impacts of this new regulation from a Notified Body’s perspective including:
- New codes of conduct for notified bodies (NB) in European market
- NB collaborations with competent authorities (CA)
- NB expectations of postmarket regulations in light of MDR
- Impact of Brexit of UK registered notified bodies