Software as a medical device: regulatory freedoms and limits
Healthcare providers and users of medical informatics should be aware when using software that it may be a certified medical device. During this event, leading experts will discuss what needs to be considered in this context.
Healthcare providers and users of medical informatics should be aware when using software that it may be a certified medical device. When does software need a CE conformity assessment, how are EU requirements evolving, what are the consequences of non-compliance and are there transition periods?
What needs to be considered when placing software on the market and when procuring software in the healthcare sector? The answers to those questions will be given at the event "Software as a Medical Device: Freedoms and Regulatory Limits", to which we would like to invite you. The event will be followed by an aperitif.
Please find the detailed event programme as well as registration details external pagehere.