Mastering GUDID registration: Your complete Guide!
Get your hands on our free eBook and checklist to learn essential information about GUDID and the registration process for your medical devices
Mastering GUDID registration!
– Let us show you how!
This eBook covers the following topics:
- What is GUDID?
- EUDAMED and FDA’s GUDID: What’s the difference?
- Checklist: How do you need to get ready for GUDID
- GUDID is just the beginning: See what countries are on the horizon and how a Global data readiness strategy can ensure future success.
Start preparing for the registration of your devices to sell your products in the US
After the GUDID (FDA) registration for medical devices of classes II and III having been mandatory for several years now, also the deadline for class I medical devices and unclassified medical devices has passed. Get ready and register your devices!
Download free eBook now
Regardless of whether you are based in the US or selling to the US market: If you want to continue selling your class I medical devices in the US, you need to register your products in time. Our eBook shows you how to get ready.
