During this workshop you will learn about the regulatory and practical side of clinical validation of medical technology. We will discuss the relevant changes in the transition from MDD to MDR, how you can prepare yourself well at an early stage and why this is so important. We discuss which clinical evidence can be used, what requirements there are to be able to do a clinical trip with a prototype or new product, and what steps are needed to set up a clinical trial.
This free workshop is complementary to the existing Techmed Workshop Serie. If you have specific questions, problems or you want more information, prepare them and use them as input for an interactive session. The supervisors are ready to help you with your prototype or product.
During this workshop, speakers from four parties will shed their light on clinical validation.
- Lisette van Steinvoren – Sr. Project Manager – Holland Innovative
- Leendert Schaake – Biomedical Engineer – Roessingh Research and Development
- Esther Spanjer – Clinical research specialist – Demcon
- Cindy Lammertink – Clinical research coordinator – University of Twente
This workshop takes place on November 13, from 4:00pm – 8:00pm. Dinner is included.
Sign up for the Techmed Clinical Validation workshop
De workshop is in English. Click here for more information and registration of this free workshop.