Gain a clear understanding of the requirements for Post-Market Surveillance and Vigilance of European Medical Devices.
This one day course is delivered by Medilink East Midlands, together with Medical Device Consultancy (MDC). The course will cover:
– 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
Delegate places are limited and selling fast. To find out more and to book your place, please click here and complete the ‘book online now’ form.
Posted on 02 June 2016