Stay Ahead of New EMC Requirements for IVD Devices | White Paper
The latest updates to IEC 61326-2-6:2025 and IEC 60601-1-2 are transforming how manufacturers approach EMC for In Vitro Diagnostic (IVD) equipment. This new paper explains what’s changing, when compliance deadlines take effect, and how to integrate EMC design and documentation strategies early to prevent costly delays. Learn practical testing insights, regulatory expectations, and how Intertek’s experts can help streamline your global market access.
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