Technical innovation requires permanently adopted legal and regulatory requirements to achieve best quality for patients, users and third.
We implement different international regulations for medical devices and In-vitro-diagnostics and comply with a wide range of regulatory requirements in many international markets with a high degree of reliability.
Our services comply with requirements as manufacturer, supplier, specification developer and consultant.
Beside others we work according to:
According to your requirements an extension of regulations is possible. Contact us!
Kontaktieren Sie uns für ein individuelles Angebot!