This one day training course by Medilink East Midlands together with Victoria Cavendish of Orca Solutions Ltd will focus on Medical Devices: Clinical Evaluations, Pre and Post-Clinical Studies.
Delegates will gain an insight into the new Medical Device Regulation and Medical Device Development with a particular focus on Clinical Evaluation, Clinical Investigation and Post Market Surveillance. There will be the opportunity for questions & discussion as well as networking.
In one day you will:
– Get up to speed with the latest Medical Device Regulation* including ISO14155
– Gain an understanding of the process & required documentation for Clinical Investigations
– Understand Post Market Surveillance including PMCF and Risk Management
*We will be holding a training course the day before this course entitled: European Medical Device Directive (MDD) Basics and Transition to the Medical Device Regulation (MDR). Both courses are complementary to one another and are taking place at the same venue and discounts are available should you or another colleague wish to attend both courses (see information below on the discounts).
To view the programme and further information (including target audience, learning outcomes and speaker profile) click on the Event Brochure link below.
Member cost: £ 200
Non-Member cost: £ 300
Discounts available:
If you would like to attend both MPD Training Courses (7 & 8 March 18), or attend one yourself and send a colleague to the other, you will save a further 20% on the delegate fee, if you have any queries please get in touch.
All prices are excluding VAT
Once we receive your booking form, you will be sent a confirmation email and an invoice.
Event Documents: