Given the popularity of medical apps and related software being used within the framework of Medical Devices and IVDs, their importance is rising annually. Along with this development it is the challenge of finding the border between software intended for wellbeing or fitness purposes and software designed for medical purposes according to MDR/IVDR.
We support you in qualifying and classifying your software by considering guidelines such as the “MDCG 2019-11 Guidance on Qualification and Classification of Software in Regulation (EU) 2017/745 – MDR and Regulation (EU) 2017/746 – IVDR” and will take care that your Medical Device Software complies with the requirements outlined in the Harmonised Standards IEC 62304 and IEC 82304.
