The New EU Medical Device Regulation

14 Jan, 2019

In May 2017, the European Commission published the new EU Medical Device Regulation (MDR) which is referred to as the most significant change to European legislation for medical devices in recent times.

In order to become compliant, medical device companies will need to adopt systems, processes and procedures. Non-compliance could possibly result in a company not being allowed to supply medical devices to the European market.

Triathlon has, with support from industry experts, identified five key success factors for the transition towards MDR compliance. The transition to MDR can be challenging, but the most successful companies could enjoy a substantial competitive advantage.

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