This conference provides an opportunity to meet Competent Authorities, Notified Body representatives, manufacturers, and a lawyer in this key area to understand and discuss the regulatory and legal requirements with respect to postmarketing surveillance.
EC Medical Device Vigilance System and Postmarketing Surveillance
Jan 24th, 2012Jan 25th, 2012
Latest in Home
Breast CT gains clinical momentum in Europe
October 16, 2025
Belgian study shows AI's promise in coronary ischemia
October 15, 2025
AI on the Aegean: EuSoMII congress comes to Crete
October 14, 2025
AI fracture detection tools tested head-to-head
October 13, 2025