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//Select CountryEnsure quality at the heart of your operations
For over 30 years, TÜV SÜD has provided market access solutions and regulatory expertise for manufacturers and suppliers of medical devices and in vitro diagnostics. Our services put your product through its paces and ensure medical device market approval and acceptance.
We have in-depth knowledge of the medical devices and IVD market and our dedicated team of over 700 experts, engineers, and medical doctors provide assessments that cover the full life cycle of your products. We are global, multilingual and have experts in all major markets who provide tailored advice for ensuring your medical devices are approved and accepted. Read more about our testing services for medical devices and IVD equipment below.
Learn about the purpose of an EMC test plan and why the IEC 60601-1-2 4th ed requires one
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Learn about the importance of biological testing and the required testing for medical devices
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The digitization of the medical sector brings with it countless opportunities.
Through a series of webinars, we will review major impacts introduced by the regulation EU 2017/746.
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Explore the In Vitro Diagnostic scope and definitions as well as the manufacturer requirements
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Understand the new regulation aesthetic manufacturers must follow and the steps to achieve compliance
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