6 May 2019
The medical device industry is undergoing a period of tremendous change.
The new Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) has been published in the Official Journal of the European Union and came into force on 25 May 2017. The transition periods for MDR and IVDR are three years and five years respectively from the date of adoption.
BSI held the seminar on MDSAP, MDR and IVDR Revision on 6 May 2019. The seminar highlighted the key changes in regulations which help the audiences consider what actions you have to start now in order to get prepared for the change in requirements.
Mr Lane Ji, Healthcare Director, BSI China
Ms Hailey Chu, Technical Specialist & Scheme Manager, BSI global IVD team