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This skill acts as a senior consultant for medical device risk management, facilitating full compliance with ISO 14971 throughout the product lifecycle. It provides expert guidance on risk analysis, hazard identification across hardware and software (IEC 62304), and the implementation of hierarchical risk controls. Users can leverage this skill to establish Risk Management Plans, perform cybersecurity threat modeling, conduct human factors use-error analysis, and maintain a comprehensive Risk Management File (RMF) that satisfies regulatory requirements for FDA and EU MDR submissions.