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.
Our Team
Marie Rogowski
REGULATORY AFFAIRS
Markus Falk
DEVELOPER
Marius Kania
REGULATORY AFFAIRS
Maria Liszyk
QA
Johannes Klein
DEVELOPER
Ruben Gallé
PRODUCT OWNER
Dr. Bassil Akra
ADVISOR
Michael M. Kania
CEO, FOUNDER
Matthias Risto
CTO, FOUNDER
Johann Töws
DEVELOPER
Fabian Muks
DEVELOPER
Daniel Laufersweiler
REGULATORY AFFAIRS
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