MDSSPRO was founded in 2016 by Patricia Vest; she has over 20 years’ experience working as an auditor and technical file assessor and reviewer for medical device companies and notified bodies across Europe including TÜV SÜD, SGS, UL and Intertek.
Our consultants are MDR specialists and are able to offer extensive, expert experience to medical device companies covering a range of subjects including software, sterilisation, electrical safety and microbiology.
Why choose MDSSPRO?
We offer quality, cost effective consultancy that meets the latest EU Medical Device Regulation (MDR 2017/745).
Client satisfaction is our top priority. We work flexibly to suit clients’ individual requirements and timeframes.
Our fees are all inclusive - there are no hidden costs.
What do our clients say about our services?
“Very interesting training, complete and with numerous examples."
"Thank you very much for this training …I learnt so much in a week."