Medical Devices On Demand Webinar

Software as a Medical Device (SaMD) and medical devices software (MDSW) has gained in importance over the last years. The new regulatory approach for SaMD and MDSW according to MDR (EU) 2017/745 is defined in the General Safety and Performance Requirements in Annex I and outlines expectations of the regulation. These requirements are defined on a high level and are very generic. Understanding relevant MDCG - Guidance documents give a clearer direction and helps to bridge the gap between regulation and practical implementation. Our webinar  "The new regulatory approach for SaMD and MDSW according to MDR (EU) 2017/745" will help you to understand possible ways of how to implement the regulation into your daily practice of software development, software manufacturing and launching it on the market considering relevant post market requirements.

Please fill out the form  to see our on demand version of the webinar.