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.

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