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13FEB2025 Webinar Slides – Closed Loop Post Market Surveillance “CLPS”
$24.99
Date: (Completed) Thursday, February 13th / 11am (USA Pacific Standard Time)
Slides presented at informative webinar on Post Market Surveillance!
Whether you’re a professional looking to expand your knowledge on the topic or learn real solutions that have been implemented, this session provided valuable insights, expert and experienced advice, and practical solutions that have proven to work through multiple audits and companies across multiple notified bodies.
What to Expect:
- Deep dive into the difference between EU MDR (EU2017 745) / IVDR (EU2017 746) requirements and US FDA 21CFR820 post market surveillance requirements.
- Slides include a consolidated process flow showing quality system elements that comprise post market surveillance and learn about the interaction that directly connects regulation requirements with procedures.
- Slides provide insight into a phased implementation approach and lessons learned from real-world examples and case studies
