Medilink East Midlands, together with Medical Device Consultancy (MDC), are offering a one day training course which will focus on Post-Market Surveillance of European Medical Devices.

Delegates will gain a clear understanding of the requirements for Post-Market Surveillance, Customer complaints and Vigilance, as well as hear about the latest updates on any new regulations.

Regulatory, Quality Assurance and Strategy Managers are encouraged to attend, as well as Regulatory Affairs attorney and other Legal Counsel. Following Case Studies, Clinical Investigations and a look at the New Regulations, there will be the opportunity for delegates to get their specific questions answered by a leading expert.

The programme will include:

• EU Regulatory Basics with Post-Market Surveillance focus, customer complaints and Vigilance
• Case Studies and Best Practice
• Clinical Investigations and Post-Market Clinical follow up
• A look at the new Regulations for Post Market Surveillance and Vigilance

Click here to find out more and book your place