Discover industry best practice for conducting clinical investigations in light of the revision to the Medical Device Directives. Hear Mhra feedback on the latest regulatory requirements for evaluations and investigations including: class III medical devices, implantables and combination products. Gain first hand feedback, advice and updates on clinical evaluation and investigation requirements from 5 Notified Bodies. Benefit from practical insights into carrying out a clinical evaluation. Enhanced networking and experience sharing opportunities with 3 new interactive sessions.