Clinical Evaluation for Medical Devices in Europe and International approach

Course targeted towards clinical project managers, clinical research associates and others working in the field of clinical investigations

Introduction
With the new Medical Device Regulations in place, it brings a whole new challenge for many companies to update their approach to gather the necessary clinical data for CE-mark. As there is no grandfathering of existing products on the market, all medical devices CE or not CE-marked are concerned about the Medical Device Regulation’s requirements immediately.
 
With these new regulations, many companies who may not have thought about the need for clinical investigations, now face an additional challenge in conducting prospective clinical investigations. Along with MDR, ISO 14155 has undergone a significant update and it’s final draft is close to being published.
 
Furthermore, the relationship companies have with their notified bodies is definitely changing, as a result of the changing climate with regards to the need for more clinical evaluation data. .

This 2-day course will provide you an in depth review of how to interpret the many changes in the clinical evaluation/investigation requirements and how to discuss aspects of clinical evaluation and investigations with the notified bodies.

Practical examples will be given in how to prepare the clinical strategy for Europe but also integrate requirements of other geographic areas such as the US, China and ASEAN countries into a global strategy.

Who should attend?
This course is targeted towards clinical project managers, clinical research associates and others working in the field of clinical investigations for medical devices.

Course language
The course will be conducted in English, alternating between lectures and studies.
  
Instructor
Danielle Giroud, CEO, WMDO (World Medical Device Organization) and CEO MD-CLINICALS

 

Excellent course leader, excellent structure, excellent that course leader had so many cases to relate to"

"Teacher is very good and topics are spot on for my current work"

Very good presenter, nice step-by-step introduction to writing CERs, nice venue and great getting the very useful slides in print"

Participants, Spring 2018

 

Indtast et "Purchase order number" hvis din virksomhed forlanger det på fakturaen.

Kontakt

mp@medicoindustrien.dks billede
Morten Petersen
Uddannelseskonsulent
49184703