The Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Training Course is an event designed to provide a comprehensive overview of the practical implications of risk management and usability, as well as an analysis of the differences between FDA guidance and MDR guidance on medical device software. Held in London, this event will bring together experts from the medical device software industry, providing a platform for exhibitors to showcase their products and services.

The sessions will cover topics such as software recalls, the use of apps in medical devices, the implications of the new draft usability standard and advice on how to validate system design. Attendees will gain valuable insights into how to comply with the EU MDR, EU IVDR and FDA regulations, as well as an understanding of the latest developments in the medical device software industry.

This event is the perfect opportunity for medical device software professionals to network and learn from industry experts. Exhibitors will have the chance to showcase their products and services to a wide range of potential customers, while visitors will gain valuable insights into the latest developments in the medical device software industry.