Implementing ISO 14971: A Practical Risk Management Guide for Medical Device Startups and Small Manufacturers (Medical Device Regulatory Foundations)
Kindle Edition or EPUB + Converted PDF نویسندگان: Mark Gour
جزئیات
فرمت: Kindle Edition or EPUB + Converted PDF تاریخ انتشار نسخه الکترونیکی : January 23, 2026
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لینک: https://www.amazon.com/dp/B0GHZHPNN7
9,799,000 تومان
زمان تحویل: حداکثر 24 ساعت
توضیحات
Implementing ISO 14971A Practical Risk Management Guide for Medical Device Startups and Small ManufacturersRisk 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.Topics covered include:Establishing a compliant risk management system, process, and filePractical hazard identification, risk analysis, and risk evaluationRisk control implementation and verificationManagement responsibility and acceptance of residual riskPost-production and post-market risk management integrationMaintaining traceability across design, manufacturing, and post-market activitiesDefending risk decisions during audits and inspectionsAligning ISO 14971 with EU MDR, FDA QMSR, and global regulatory expectationsThe guide incorporates European regulatory expectations through EN ISO 14971:2019/A11:2021 and explains how benefit-risk justification, residual risk, and post-market information are evaluated in practice.Written by a former medical device manufacturer and quality system leader, this book is intended for founders, engineers, and quality and regulatory professionals who are responsible for making and defending risk-based decisions.If you are looking for a clear, practical approach to ISO 14971 that goes beyond theory and survives real audits and inspections, this guide is written for you.
9,799,000 تومان
زمان تحویل: حداکثر 24 ساعت