EBOOK

CE marking guide for medical devices in the EU

An overview of the CE marking process for medical device manufacturers in the European Union, and the associated technical documentation/general safety and performance requirements (GSPRs) that manufacturers are required to maintain.

More infoWatch ReplayGet the ebookGet the briefGet the case studyGet the data sheetGet the webinarGet the video
CE marking guide for medical devices in the EU

Get the ebook

Get the case study

Get the webinar

Watch the replay!

Get the video

Get the data sheet

Thank you! Here's a link to your resource. We've also sent a copy to your inbox. Enjoy!
Thank you! We've sent you you details about accessing this event. If you do not receive an email in the next few minutes, please check your spam folder. Enjoy!
Download
Here's some additional content you may find helpful
A primer on medical device classification
A primer on medical device classification
5 ways a RIM system can accelerate time-to-market for MedTech companies
5 ways a RIM system can accelerate time-to-market for MedTech companies
Quick reference guide - global medical device UDI requirements and timelines
Quick reference guide - global medical device UDI requirements and timelines
Here's your video, enjoy!
Check out these additional resources
A primer on medical device classification
A primer on medical device classification
5 ways a RIM system can accelerate time-to-market for MedTech companies
5 ways a RIM system can accelerate time-to-market for MedTech companies
Quick reference guide - global medical device UDI requirements and timelines
Quick reference guide - global medical device UDI requirements and timelines
Oops! Something went wrong while submitting the form