
Post-Market Surveillance under MDR
This webinar provides essential information to better understand post-market surveillance requirements under MDR (EU) 2017/745, including clinical follow-up, complaints, vigilance, and collaboration with external operators.
Date
9 April, 2026
Time
17:30-18:30 CET
Registration Deadline
7 April, 2026
Typology
Live Streaming
Language
Italian
Pricing
Free

Post-market surveillance, which includes clinical follow-up, complaints, and vigilance, is an essential process to ensure compliance with the product and quality management system requirements established by MDR (EU) 2017/745. It also involves collaboration with external operators outside the organization. This webinar, in collaboration with JOB ON BEAUTY, provides a comprehensive overview of the key requirements and practical insights needed to effectively implement this process.










