Despite the delay of EU MDR into May 2021, some organisations are still burning valuable time in terms of updating the labelling and instructions for use of their medical devices. Bob Tilling at Kallik shares his experience from recent customer projects and explains how medical device manufacturers can recover lost time in preparing EU MDR labelling and IFU compliance.

[gview file=”https://www.ipimediaworld.com/wp-content/uploads/2021/04/EU-MDR-Changes-are-Only-the-Beginning-–-Ensure-IFU.pdf”]