As an engineer or developer, you know: In the highly regulated environment of the medical device industry, completely different requirements apply than in many other sectors.
For you, this means that you must be familiar with all the details of the Medical Devices Directive and the harmonized standards and, above all, be able to apply them.
Our experienced trainers will train you in this complex set of regulations - with solid theory and practical examples. We are trained in life cycle processes, software development and therefore safety-oriented development and everything that needs to be considered in terms of standards.
SGS-TÜV Saar GmbH
Benzstr. 28
D-82178 Puchheim near Munich
t: +49 89 787475 – 283