Accelerate Your Entry Into New Markets

Accelerate Your Entry Into New Markets

Manufacturers in the competitive and rapidly growing global medical device industry face constant demands for product innovation.

New products must guarantee high-quality performance and complete safety to achieve regulatory approval and global market access. With the highest number of medical device experts and the most comprehensive service offering of any Notified Body (NB), our team is ready to support companies of all sizes.

Download E-Book

If you have any questions regarding our services, please email [email protected].

Contents of this E-Book include:

• Aligning your innovation with changing regulations
• Portfolio – Testing services, inspections, audits, and system certifications
• Industry Accreditation
• Why choose TÜV SÜD

Did you know?

We are a technology leader with 400 experts based in major markets across the globe, the most in the industry. TÜV SÜD possesses a Regulatory Foreign Affairs & Clinical Department specializing in market access and worldwide regulations, ensuring that each client’s products are tested to comply with the latest requirements.