Flinn careers

With a new EU regulation, it's becoming much more difficult to keep track of all regulatory requirements for medical device producers - no matter if they produce defibrillators, pace makers, masks or contact lenses.
In response, we are working on a software-and-a-service platform that should make compliance submissions far more straightforward through the use of automation for a variety of repetitive form filling workflows. Each workflow would be orchestrated from a single platform, reducing the "complexity and cost".