EU Postmarket Surveillance Requirements for Medical Devices

[@Daithi-o4m]

Very enjoyable Rob. Nicely put together.

[@MedicalDeviceAcademy]

Thank you.

[@marcealizaga7195]

I'm a professional in the medical device industry and was looking for an overview on PMS. This resulted to be a great resource! I also really liked the way you explained everything and keeping my interest all the way. Any other webinars that you could recommend for me to dig into? As part of my development plan I'm seeking to grow my knowledge in the PMS area, would like to better understand what PMS is and does as a whole.

[@MedicalDeviceAcademy]

There are 5 other videos about PMS on our channel. Here's one of the them: kzbin.info/www/bejne/bYLRhZ55oal4itk. We will also be offering a PMS webinar later this year that will cover ISO/TR 20416 and our procedure (SYS-019).

[@华英何]

Can I have A common PMS report for class A and class B devices? Because only PSUR requires every device for class c and class D, right?

[@MedicalDeviceAcademy]

PMS reports should be specific to a product or product family. Therefore, if you have two different classifications, you should have two different reports.