With over 40 years of expertise and capabilities, Eurofins Medical Device Services offers comprehensive solutions across the entire medical device lifecycle. Through our global network of regulatory and toxicology experts, laboratories, and sterile packaging sites in Europe, North America, and Asia Pacific, we help manufacturers achieve compliance and market readiness.

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Tuesday, May 20, 2025

Usability techniques for compliance: the use of Annex C of IEC 62366 News

IEC 62366-1 (2007) defines usability requirements for medical devices to reduce user-related risks and ensure safe, effective device use.

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