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Healthcare and Medical Device Services

 

For over 30 years, TÜV SÜD has provided certification and testing services for manufacturers and suppliers of medical devices and in-vitro diagnostics.
We have in-depth knowledge of the medical devices and IVD market, and our global team of experts provides assessments covering your products' entire life cycle.

TÜV SÜD’s global team of over 750 healthcare and medical device testing experts, engineers and medical doctors are well positioned to help your testing run smoothly, stay informed about the new regulatory requirements, and best prepare your device to reach market quickly.

Find out more about the services we provide for the healthcare industry and medical device manufacturers.

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UKCA Requirements for Medical Device Manufacturers
Webinar

UKCA Requirements for Medical Device Manufacturers

General guidance on the UKCA conformity assessment process

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The New Medical Device Regulation (MDR)
Infographics

The New Medical Device Regulation

Extended transition period ends on May 26, 2024 for devices with valid MDD/AIMDD certification

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AI in medical devices
White paper

Artificial Intelligence in Medical Devices

Verifying and validating AI-based medical devices

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EU MDR
Webinar

EU MDR and its impact on cardiovascular manufacturers

How to ensure a smooth transition to MDR certification.

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