EC 62304 defines a framework for life cycles of MP software. Mostly traceability matrices are used to prove a compliant development – especially for large systems it becomes challenging. We show you how the use of digital tools can support this process as well as seamless integration into risk management and thus accelerate approval.

Our experts for the convenient generation of technical documentation for medical devices will show you the most important functions live on the system free of charge on 09 February 2021 from 10.30 to 11.30 am and will be available to answer your individual questions.

Register now: