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Our experts have the deep knowledge to assess medical devices from our partners.
Common challenges in the medical devices industry
Irregular interpretation of standards and requirements
TÜV SÜD assesses medical device manufacturers products for compliance and regulatory standards that vary from country to country.
Rapidly advancing technology
Medical technology is advancing rapidly, especially with the rise of AI. We assess innovative technologies in the medical field to verify regulatory compliance.
Maintaining quality
We maintain quality by ensuring that all TÜV SÜD laboratories are ISO 17025 accredited to service our clients.
Unpredictable market access to EU
We set clear expectations with our partners to overcome the unreliable timing.
Integrating several test houses
TÜV SÜD is a global partner for medical devices testing services including microbiology, chemistry, electrical, physical testing and more.
Time-consuming coordination of all laboratories
TÜV SÜD’s dedicated project handler will be your single point of contact for all tests.
TÜV SÜD's service portfolio for the medical devices industry
As the medical devices industry serves billions, regulatory requirements will increase. TÜV SÜD will be with you every step of the way.
Research and development require prototypes to undergo stringent and rigorous testing for quality, durability, and safety for use in or on the human body. Our experts test components, raw materials, prototype creations, and final medical devices to ensure that they adhere to the highest standards.
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