Navigating regulatory challenges across the life cycle of a SaMD.

Abstract

Software as medical devices (SaMDs) have become part of clinical practice and the management of the development and control processes of the documentation associated with them are an integral part of many medical realities. The European Regulation, MDR (EU) 2017/745, introduces a classification rule (rule 11, Annex VIII) specifically for software, which provides more explicit requirements than in the past, leading to classification of many software to higher risk and therefore to more complex ce