Clinical Evaluations & Investigations for Medical Devices 2014
April 8 - 9, 2014
ダブリン , アイルランド
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.
2014 Speaker faculty includes
John O'Dwyer European Manager NSAI
Gert Bos Head of Regulatory & Clinical Affairs, Healthcare Development BSI Product Services
Alexander Cristea Head of Clinical Affairs Episurf Medical ABS, Sweden
Laurie Clark Partner King & Spalding
Dr Nurcan Coskun District Manager, International Clinical Operations Medtronic, Switzerland
and many more...
2014 Speaker faculty includes
John O'Dwyer European Manager NSAI
Gert Bos Head of Regulatory & Clinical Affairs, Healthcare Development BSI Product Services
Alexander Cristea Head of Clinical Affairs Episurf Medical ABS, Sweden
Laurie Clark Partner King & Spalding
Dr Nurcan Coskun District Manager, International Clinical Operations Medtronic, Switzerland
and many more...
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Clinical Evaluations & Investigations for Medical Devices April 8 - 9, 2014