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Implementing ISO 14971: A Practical Risk Management Guide for Medical Device Startups and Small Manufacturers. Risk management is one of the most scrutinized and most misunderstood aspects of medical device compliance. Regulators do not assess risk management based on templates or completed forms. They assess whether risk-based decisions are logical, justified, and maintained across the entire device lifecycle. Implementing ISO 14971 is a practical, implementation-focused guide written for startups and small medical device manufacturers who must build and defend risk management systems with limited resources. It explains how ISO 14971 is applied in real operating environments and how regulators and auditors review risk management evidence during audits and inspections. This book does not restate the ISO 14971 standard or reproduce normative text. Instead, it focuses on how to establish, maintain, and defend a proportionate, audit-ready risk management system that integrates with an ISO 13485 quality management system. (Amazon) Key topics: Topics covered include: Establishing a compliant risk management system, process, and file; Practical hazard identification, risk analysis, and risk evaluation; Risk control implementation and verification; Management responsibility and acceptance of residual risk; Post-production and post-market risk management integration; Maintaining traceability across design, manufacturing, and post-market activities; Defending risk decisions during audits and inspections; Aligning ISO 14971 with EU MDR, FDA QMSR, and global regulatory expectations. The guide incorporates European regulatory expectations through EN ISO 14971:2019/A11:2021 and explains how to demonstrate compliance with General Safety and Performance Requirements (GSPR). (Amazon)