We like to share our experiences regarding MDR, ISO13485 and Risk Management. We would like to invite you to our training sessions on these topics, which we can hold on site and adjust to your specific needs so that the training session will cover the information you are looking for. In addition, we regularly offer training sessions for which you can sign up using the button below. Please keep an eye on our training schedule, and reach out to us for more information on training sessions.

MDR and QMS training for software as a medical device

Following several succesfull editions, we are hosting a new Medical Device Regulation (MDR) and Quality Management System (QMS) training on the 7th of December 2023.

Medical Device Regulation & ISO13485 training

Following two very successful editions of the training in 2022 we are hosting the 3rd edition of the Quality Management System (QMS) and Medical Device Regulation (MDR) training soon. Together with our partner Medace we are organizing the QMS and MDR training on June 14, 2023. In order to ensure the training will be interactive limited spots are available. Click here to register.