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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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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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Medical Device Design

Medical Device Design: Innovation from Concept to Market, Second Edition provides the bridge between engineering design and medical device;

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FDA Regulatory Affairs

development, research, manufacturing, and marketing. The Second Edition focuses on the new drug approval process, cGMPs, GCPs, quality system;

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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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International Medical Device Clinical Investigations: A Practical Approach, Second Edition

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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Medical Device Technologies

Medical Device Technologies: A Systems Based Overview Using Engineering Standards, Second Edition, is a comprehensive overview of medical;

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Guide to Microbiological Control in Pharmaceuticals and Medical Devices

microbiological integrity. Updated to reflect technological and regulatory changes, the Guide to Microbiological Control in Pharmaceuticals and Medical;

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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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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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Plastics in Medical Devices

anywhere else. Comprehensive coverage of uses of polymers for medical devices Unique coverage of medical device 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 Packaging Handbook

This volume details current developments in industry practices and standards relating to medical device packaging. This edition offers;

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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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Safety Risk Management for Medical Devices

Safety Risk Management for Medical Devices, Second Edition teaches the essential safety risk management methodologies for medical;

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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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Pharmaceutical Dosage Forms

Completely updated and enlarged to three volumes (originally published as two volumes), the Second Edition of Pharmaceutical Dosage Forms;

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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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