With our consulting and services you can be sure that you comply with all legal requirements regarding the Medical Device Regulation MDR Service EN. For us, service means that, if required, we will take over all tasks relating to material reporting for medical devices for you: a convenient complete service for you, so that you no longer have to worry about anything.

However, you can also book our services on a modular basis, depending on how you need them. Our many years of experience in working with companies from a wide range of industries enable us to provide both manufacturing and supplier companies and distributors with the right help in the area of material compliance quickly and in a targeted manner.

The management of material compliance data including data entry, administration and maintenance are responsible tasks, because mistakes can quickly lead to legal consequences. In addition, you miss many opportunities to organize your business processes more efficiently and in a more modern way if you do not yet have access to important up-to-date information or knowledge about the latest developments.

It often makes sense to outsource certain tasks or entire processes in the area of material compliance and persistent organic pollutants. With our comprehensive service, we accompany all tasks in the area of product compliance to long-lived organic pollutants: from the conception to the implementation of projects. Here, you can rely on our experience and hands-on mentality and the smart, precise working methods of our Expert:innen team.

Use our contact form for an initial free consultation!