2017 - MDTI - Medical Device School

The Medical Device School is an ideal opportunity for delegates to get to grips with the entire medical device product life-cycle, covering everything from research and development to gaining regulatory approval and getting your product to market. It is also an opportunity to discover how the new Medical Devices Regulation will impact you in your job role.
Highlights
-Gain valuable updates and insight into the new Medical Device Regulation (MDR)
-Our School includes 5 interactive learning sessions on: Classification, Risk Management, Biocompatibility, Vigilance and Reimbursement
-With 10+ speakers you will share experiences with some of the most highly respected professionals in the field
Key Benefits
-Understand and explore the latest changes in legislation surrounding the new Medical Device Regulation (MDR)
-Learn the fundamentals of device regulations such as classification and conformity assessment
-Discover how to conduct a biological evaluation
-Examine the importance of having a robust risk management plan
-Gain an insight into clinical investigations for devices
-Understand the need of having a quality management system in place
-Discover optimal reimbursement strategies to get your device paid by healthcare providers such as the NHS
-Gain an insight into post market surveillance and vigilance to ensure your devices continue to be safe on the market