Location: Frankfurt, Germany

Description: The event will provide insight into practical solutions implemented by medical device companies to determine the appropriate level of evidence needed, and to develop plans to meet enhanced Post-Market Clinical Follow-up requirements. Focused working groups and peer-to-peer discussion will allow for the sharing of strategies to optimise cost-effective data collection while addressing challenges relating to registry data ownership, privacy concerns, physician motivation, and much more.

Organiser: Q1 Productions

Contact: +1 312 955 0424