WebForm Medical Devices
The In Vitro Diagnostic Regulation (IVDR 2017/746) introduces new rules for the regulation of in vitro diagnostic devices in the European Union (EU). Are you aware of all the changes and new requirements for your products? Are you ready to implement them to your company?
Sometimes adapting to changes is complex, and we do not become aware of how it happens to us. Even more when we are in a regulation context.
An expert editor has created this free checklist where filling in our questionnaire you will find out what is the level of compliance of your processes and products. After it you will receive the quick feedback of your needs from the experts of Ambit BST.