This one day training course by Medilink East Midlands together with Medical Device Consultancy will provide you with an introduction to current Medical Device Regulation in the European Union.
Some of the items that will be covered during this course are:
– How to classify your medical device
– Conformity assessment procedures
– Technical documentation
– Post Market Surveillance
To view the programme and further information, click the ‘Event Brochure’ link below.
To book your place, please complete the ‘book online now’ form below.