This one day training course by Medilink East Midlands together with Medical Device Consultancy (MDC) will be an excellent opportunity to learn about the European MDD and MDR basics and the differences between the two.
Find out what impact the MDR will have and the key considerations you need to be aware of, including all timescales.
This training course will also cover:
– How to classify your Medical Device
– How to choose the Conformity Assessment Routes under the MDR
– Compiling your technical documentation for a Medical Device
– How to label your Medical Device
– Clinical Evaluations of Medical Devices in the EU
The final session of the course will cover key considerations for the MDD to MDR Transition, including suitable action plans.
To view the programme and further information click on the Event Brochure PDF below.