Testimonials

“It was fascinating to get first-hand insights into the uncertainty in the medtech sector. It became clear that although the pharmaceutical industry and the medical technology sector have the same goals - always with a focus on patient safety – there are nevertheless different approaches in some areas. As part of my continuing education, I learned how quality is ensured during medical technology product development. The programme offers an ideal combination of project and quality management, especially for those who want to acquire broad expertise in medical technology. It was particularly valuable to have the chance to deal in depth with a topic of my own choosing as part of the final thesis. The face-to-face discussions with my supervisor also greatly enriched the programme”.

“The main topics of clinical affairs, regulatory affairs and quality assurance for medical devices & in-vitro diagnostics were presented in an exciting and multifaceted way. It was great to have so many different lecturers who have all had profound experience in the industry. I also found it very helpful that we had interactive exercises on each day of the course, where we could directly apply and try out the things we had learned. In addition, the class size of around 15 people was perfect, as was the fact that the participants had such a variety of backgrounds. This made it possible to learn from each other in the exercises and discussions, and to get an insight into how problems are solved in other companies. For these reasons, I can strongly recommend the CAS CARAQA programme to anyone who is active in this field”.