Is your organization ready for the new data demands in the wake of the medical device regulation?

Is your organization ready for the new data demands in the wake of the medical device regulation? Do you know how to build up timely clinical evidence and safety documentation for medical device lcm and market access? This course hosted by MEDICOINDUSTRIEN introduces the concept of real-world evidence (RWE) for medical device products.

Full program available at https://lnkd.in/g6AkBbc

2019-03-25T10:43:33+00:00 March 25th, 2019|Categories: Uncategorised|