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 5 (of 6) of the webinar series "The New EU Medical Device Regulation".
Date: 06.09.2018 Time: 16.00 - 17.00 CET
AGENDA Topics covered
Clinical testing requirements
Effect of the new MDR on class I,IIa, IIb and III devices
Technical documentation requirements and vigilance
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.