In 2012 the EU commission adopted a package of measures on innovation in health, consisting of a communication and two regulation proposals to revise existing
legislation on general medical devices and in vitro diagnostic medical devices.
Equip your professionals with all details of this new regulation in a series of 6 webinars.
Part 2 (of 6) of the webinar series "The New EU Medical Device Regulation".
Date: 02.08.2018 Time: 16.00 - 17.00 CET
AGENDA Topics covered
Class I and IIa devices
Effect on class IIb devices
Class III devices
WHO should attend
Clinical Trial Managers
Regulatory Affairs Professionals
WHY you should attend
Because the current directive will be significantly altered
...and replaced by a regulation which is legally binding on all EU member states.