MDTI - Medical Device School 2017

Topics

• Classification
• New Medical Device Regulation (MDR)
• Biocompatibility
• Risk Management
• Reimbursement
• Vigilance
• Fundamentals of device regulations such as classification and conformity assessment
• The latest changes in legislation surrounding the new Medical Device Regulation (MDR)
• The importance of having a robust risk management plan
• How to conduct a biological evaluation
• The need of having a quality management system in place
• Clinical investigations for devices
• Post market surveillance and vigilance to ensure your devices continue to be safe on the market
• Optimal reimbursement strategies to get your device paid by healthcare providers such as the NHS

Who should Attend

Attendees involved or interested in broaden their knowledge of the medical devices industry, such as:

• Graduate
• Existing employee
• New to an area/department
• somebody who would benefit for future career development