Date: 16 & 17 May 2018
Location: Thon Hotel, Brussels, Belgium
Language of instruction: English
Theme: Transitioning to the New EU MDR and IVDR
This two-day workshop explores the most important current concerns regarding the transition to the latest EU regulatory expectations for medical devices and IVDs, as introduced by the new Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR).
For more information and subscription, please check the website of RAPS.