MDR (EU) 2017/745 – Post-Market Surveillance

MDR (EU) 2017/745 – Post-Market Surveillance

This seminar provides the essential skills to understand the key requirements of post-market surveillance under MDR (EU) 2017/745.

Date

10 September, 2026

Registration Deadline

3 September, 2026

Format

8-hour courses — Live streaming

Language

Italian

Price

€580 for non-clients
€435 for clients — VAT excluded

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Post-market surveillance, which includes clinical follow-up, complaints, and vigilance activities, is a key process for meeting the product and quality management system requirements set out in MDR (EU) 2017/745, also through collaboration with operators external to the organization.

This seminar provides the necessary skills to understand the key requirements of this process.

Program

Managing the post-market surveillance (PMS) process
Elements of reactive PMS
Elements of proactive PMS
PMS/PSUR plan and report, trend analysis
Monitoring and communication activities with competent authorities: vigilance
Event reporting, field corrective actions, and recall management
PMCF plan and report

The seminar includes

MDR Toolkit (experience, templates and tools)
Educational tutor support
Training materials
Skills assessment test
Certificate of attendance

Seminars are available for individual purchase, but they are also included in our Advanced Master and MDR Course training programmes, which offer more comprehensive learning paths and greater overall cost advantages.

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