Medical Devices
Bring your innovations to new markets
The medical device industry is powered by innovation. New and converging technologies are driving breakthroughs in medical device development every day. To stay on top of the market, each new product must achieve regulatory approval and market entry. This requires an innovative process that cuts product development time and ensures consistently high performance.
TÜV SÜD’s experts have refined this process for you. We offer comprehensive global compliance services that ensure your products’ market acceptance and success. And we know the importance of time. For example, we offer a unique service that guarantees your initial assessment of the application for CE-marked class III devices is completed within 60 days.
We assist you during all phases of medical device production and identify potential risks. From the first idea to market launch, our extensive network, coupled with high-tech laboratory infrastructure, ensures a smooth development process and certification procedure.
We have the most competent personnel available. They are qualified for the highest risk products, including a dedicated team of medical doctors to assess clinical data. By combining this expertise with global experience, we guarantee your medical devices reach the highest quality and safety standards.
Our services at a glance
Your benefits at a glance
- Improve your process quality and transparency
- Ensure quality, safety and performance of your devices
- Raise brand reputation and consumer trust and satisfaction
- Avoid costly product recalls by delivering consistent quality and safety