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Handbook of Medical Device Regulatory Affairs in Asia: Second Edition

Medical device regulation in Asia has gained more importance than ever. Governments and regulatory bodies across the region have put;

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Handbook of Medical Device Regulatory Affairs in Asia

Medical device regulation in Asia has gained more importance than ever. Governments and regulatory bodies across the region have put;

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Medical Regulatory Affairs

First handbook in the market to cover regulatory affairs in Asia. This handbook covers medical device regulatory systems in different;

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Medical Device Safety

proposed. An essential book for all those involved in health physics, engineering, and medical regulatory affairs.;

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Medical Device Regulatory Practices

This book is intended to serve as a reference for professionals in the medical device industry, particularly those seeking to learn from;

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Humanizing Healthcare Human Factors for Medical Device Design

regulatory affairs. Teaches readers to design medical devices that are safer, more effective, and less error prone; Explains the role and;

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Humanizing Healthcare - Human Factors for Medical Device Design

regulatory affairs. Teaches readers to design medical devices that are safer, more effective, and less error prone; Explains the role and;

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Cost-Contained Regulatory Compliance

This book guides the reader through FDA regulation guidelines and outlines a comprehensive strategy for cost reduction in regulatory;

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Cybersecurity for Connected Medical Devices

Quality Management Systems (QMS). This book is geared towards engineers interested in the medical device cybersecurity space, regulatory, quality;

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Medical Device Quality Assurance and Regulatory Compliance

Acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents;

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Medical Device Quality Assurance and Regulatory Compliance

Acquaints developers of medical devices with the basic concepts and major issues of medical quality assurance and regulatory documents;

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Medical Technology In Japan

of Japan's medical field to make sense of the state of the country's medical profession and its regulatory framework. She explores the development;

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Medical Technology in Japan

of Japan's medical field to make sense of the state of the country's medical profession and its regulatory framework. She explores the development;

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A Simple Guide to Understanding Medical Device Regulations

has also led to an increase in costs associated with licensing where required. Regulatory controls for medical devices are often complicated;

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Medical Product Regulatory Affairs

regulatory affairs in all major global markets for pharmaceuticals and medical devices. Following a look at drug development, complete sections are;

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Medical Device Design

This book provides the bridge between engineering design and medical device development. There is no single text that addresses the;

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Usability Testing of Medical Devices

publication of the first edition, the FDA and other regulatory groups have modified their regulations and expectations regarding how medical device;

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The Medical Device R&D Handbook

Exploring the practical, entrepreneurial, and historical aspects of medical device development, this second edition of The Medical Device R;

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Understanding Medical Devices

examples of various medical devices, the essential principles of safety and performance, the use of standards by the regulatory bodies, the various;

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FDA Regulatory Affairs

Regulatory Affairs: provides a blueprint to the FDA and drug, biologic, and medical device development offers current, real-time;

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Handbook of Medical Device Design

First published in 2001: This handbook has been written to give those professionals working in the development and use of medical devices;

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Handbook of Medical Device Design

First published in 2001: This handbook has been written to give those professionals working in the development and use of medical devices;

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Medical Device Quality Management Systems

of quality, compliance, and regulatory professionals in medical device companies. It includes secrets for developing an effective, yet efficient;

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Medical Device Design

improving older ones; this book fills that need. It addresses medical devices' regulatory (FDA and EU) requirements, shows the essential;

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Foundations and Strategies for Medical Device Design

communicating and understanding the scientific, regulatory, and business aspects of medical device design. Foundations and Strategies for Medical;

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International Medical Device Clinical Investigations

The demand for clinical evidence has become an increasingly important issue in the development of medical devices. This demand is reflected;

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FDA Regulatory Affairs

FDA Regulatory Affairs is a roadmap to prescription drug, biologics, and medical device development in the United States. Written in plain;

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