Who are you?

You are a medical device project manager who wants to develop in a modern and agile way while maintaining a design history file in a consistent manner.
You are a RA/QA engineer who wants to keep up with the development team while ensuring the documentation follows your proedures.
You are in a startup and you just discovered that generating the documentation needed for the CE marking or FDA 510(k) will be more complicated than you thought, and you could use some help to streamline that effort.
Or perhaps you are a RA/QA consultant and you work with customers who lack some good workflow for their documentation process...

How can we help you?

Being project managers in medical devices companies for many years we experienced firsthand how industry changed from the waterfall to a v-model and now a very agile product development. As the product development methods evolved we were struggling more and more to keep an up-to-date documentation to match our agile teams.
Since we could not find a tool on the market that was easy enough yet powerful, we decided to create our own. Later came the idea that it could be used by a lot of other companies: Matrix Requirements was born.

Our goal is to help people create better medical devices with less working hours consumed by documentation. We accomplish this with our proprietary software tools, training about relevant standards, and by building a long-lasting relationship with our customers so that they can achieve their ambitious goals. We like to compete on usability and customer service. We are eager to work with you on your next challenge.
Customers

Who are we?

Headquarters

Matrix Requirements GmbH

Phone:
Blumenstrasse 9a
77704 Oberkirch, Germany

Belgian Branch

Make It Real sprl

Phone:
15 avenue des Princes Brabançons
1170 Watermael-Boitsfort, Belgium

US Branch

Product Realization Group

Phone:
433 Concord Drive,
Menlo Park, CA 94025
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