These people work hard every day to simplify regulatory life and bring more joy to your workplace.
Made in Fulda, Germany. Hosted in Frankfurt and around the globe. Right there where you need it. The story of meddevo begins as early as 2016, when the idea was formed to develop a solution exclusively for medical devices and IVDs. The requirements of the EU-MDR and IVDR were only one benchmark. Over the years, meddevo developed into an all-rounder in the regulatory world. Not just a software solution, but a dynamic and flexible platform.
So that the software adapts to the requirements of the manufacturer and not the other way around. meddevo is getting a little better every day. Our customers are of course pleased about that. And very soon you will be able to access top experts from the industry via meddevo. Right when you need them.