The ISO 10993 series of standards covering biological evaluation of medical devices is well established and regulatory authorities worldwide expect compliance. In Europe, compliance with the standards is the easiest way to meet the general safety and performance requirements of the MDR, and understanding a risk management approach to biological safety is essential. This seminar will provide key guidance on how to use the standards and successfully apply a risk management approach to the biological evaluation of medical devices. The event, which will be held at the Rembrandt Hotel in London, UK, is organised by Management Forum (+44 (0)20 7749 4730).london