Free Medical Device Post-Market Surveillance Course: Concepts
Dr. Oliver Eidel
·
IEC 62304: Medical Device Software Development
·
Published December 27, 2025
In this video we will dive into the concept of post-market surveillance. We will see how the reactive and pro-active surveillance of field data update the risk-management and the clinical evaluation.
Looking for an eQMS software for medical device compliance? Check out our eQMS, Formwork, the best eQMS for lean, founder-led companies:
https://openregulatory.com/
Looking for an eQMS software for medical device compliance? Check out our eQMS, Formwork, the best eQMS for lean, founder-led companies:
https://openregulatory.com/
Keep watching
All videos
5:16
Medical Device Post-Market Surveillance: The Process
Dr. Oliver Eidel
25 views
·
5 months ago
12:34
Medical Device Post-Market Surveillance: The Plan
Dr. Oliver Eidel
24 views
·
5 months ago
6:23
Post-Market Surveillance: The Periodic Safety Update Report (PSUR)
Dr. Oliver Eidel
30 views
·
5 months ago
I’m a medical doctor, software engineer and regulatory dude. I’m also the founder of OpenRegulatory.
Through OpenRegulatory, I’ve helped 100+ companies with their medical device compliance. While it’s also my job that we stay profitable, I try to dedicate a lot of my time towards writing free content like our articles and templates. Maybe that will make consulting unnecessary some day? :)
If you’re still lost and have further questions, reach out any time!
Through OpenRegulatory, I’ve helped 100+ companies with their medical device compliance. While it’s also my job that we stay profitable, I try to dedicate a lot of my time towards writing free content like our articles and templates. Maybe that will make consulting unnecessary some day? :)
If you’re still lost and have further questions, reach out any time!
Join the discussion. Leave a comment. Guest comments are welcome — add your email to get reply notifications.
No comments yet. Be the first to share your thoughts.