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Safety Risk Management for Medical Devices, Second Edition teaches the essential safety risk management methodologies for medical devices compliant with the requirements of ISO 14971:2019. Focusing exclusively on safety risk assessment practices required in the MedTech sector, the book outlines sensible, easily comprehensible, state-of the-art methodologies that are rooted in current industry best practices, addressing safety risk management of medical devices, thus making it useful for those in the MedTech sector who are responsible for safety risk management or need to understand risk management, including design engineers, product engineers, development engineers, software engineers, Quality assurance and regulatory affairs. Graduate-level engineering students with an interest in medical devices will also benefit from this book. The new edition has been fully updated to reflect the state-of-the-art in this fast changing field. It offers guidance on developing and commercializing medical devices in line with the most current international standards and regulations. Key topics: - Includes new coverage of ISO 14971:2019, ISO/TR 24971\n- Presents the latest information on the history of risk management, lifetime of a medical device, risk management review, production and post production activities, post market risk management\n- Provides practical, easy-to-understand and state-of the-art methodologies that meet the requirements of international regulation\n- Editorial Reviews / From the Back Cover: Fully updated to cover ISO 14971:2019, ISO/TR 24971, Medical Device Directive (MDD) and Active Implantable Medical Device Directive (AIMDD) requirements.