The increasing interconnection of medical devices exposes manufacturers to new responsibilities—often unforeseen and sometimes poorly understood. Cybersecurity is not an add-on, but a regulatory requirement that calls for robust evidence, appropriate testing, and impeccable documentation.

Together with experts from Complife Group and TÜV Rheinland, we will analyze which devices are most vulnerable, what Notified Bodies expect, why testing is often unavoidable, and what the main gaps identified in Technical Documentation are.

A free webinar aimed at spreading awareness and preparing manufacturers for a topic set to become increasingly central.

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