QUNIQUE: Call the Experts
If you’re preparing your company for the new Medical Device Regulation (MDR) and need support on how to comply to the new requirements, call the experts at QUNIQUE.
The MDSAP Medical Device Single Audit Programme Practical Training for Medical Device Manufacturers is taking place on 21 March.
QUNIQUE presents its seminar and workshop 'Medical Device Regulation (MDR) Performing Successful Clinical Evaluation', which will take place on the 11 January 2018 in Zurich...
Make an enquiry
Thank you for submitting the form. Your enquiry will be submitted to the company.