MDSSPRO’s medical device regulatory training workshops
Our training courses are suitable for large or small medical device companies – from global corporates to specialist manufacturers. Courses are tailored to the individual requirements of companies and range from week long courses to one day workshops.
Training in specific medical device regulatory requirements cover the following topics (click on the photos below to see the title appear):
The training sessions can be held at clients’ offices, at an independent venue or remotely by access to a platform (e-learning).
The interactive e-learning training workshops includes a presentation of MDR requirements, the structure of MDR, conformity assessment routes, general safety and performance requirements, classification and clinical evaluation.
The workshop is supported by an online trainer and includes skill practice sessions and tests. A certificate is delivered at the end of the training.
For more details on the training sessions available contact us at firstname.lastname@example.org.
For registration to our training courses please complete the form below: