Encyclopedia of Medical Devices and Instrumentation, 6 Volume Set, 2nd Edition, John G. Webster
Автор: Dennis Fitzpatrick Название: Implantable Electronic Medical Devices, ISBN: 0124165567 ISBN-13(EAN): 9780124165564 Издательство: Elsevier Science Рейтинг: Цена: 70740.00 T Наличие на складе: Есть Описание: Provides a background on the application of medical devices, an introduction to the latest techniques used and a case study of existing medical devices. This book can be used as a guide to the design of medical devices and also as a reference for existing medical devices.
Автор: Peter Armitage and Theodore Colton Название: Encyclopedia of Biostatistics (8 Volume Set) ISBN: 047084907X ISBN-13(EAN): 9780470849071 Издательство: Wiley Рейтинг: Цена: 3607830.00 T Наличие на складе: Поставка под заказ. Описание: Covers statistical issues pertinent to life scientists, healthcare professionals and practising statisticians. This title is suitable for those involved in statistical activities in medicine and health sciences.
Название: Guidelines for Falure Modes and Effects Analysis for Medical Devices ISBN: 0849319102 ISBN-13(EAN): 9780849319105 Издательство: Taylor&Francis Цена: 296030.00 T Наличие на складе: Невозможна поставка. Описание: Presents guidelines that focus on failure modes and effects analysis (FMEA) and its application throughout the life cycle of a medical device. This book outlines the major US and EU standards and regulations. It presents an overview of risk management and risk analysis methodologies, and common FMEA pitfalls.
Автор: Fiedler, Beth Ann Название: Managing Medical Devices within a Regulatory Framework ISBN: 012804179X ISBN-13(EAN): 9780128041796 Издательство: Elsevier Science Рейтинг: Цена: 131380.00 T Наличие на складе: Есть у поставщика Поставка под заказ. Описание:
Managing Medical Devices within a Regulatory Framework helps administrators, designers, manufacturers, clinical engineers, and biomedical support staff to navigate worldwide regulation, carefully consider the parameters for medical equipment patient safety, anticipate problems with equipment, and efficiently manage medical device acquisition budgets throughout the total product life cycle.
This contributed book contains perspectives from industry professionals and academics providing a comprehensive look at health technology management (HTM) best practices for medical records management, interoperability between and among devices outside of healthcare, and the dynamics of implementation of new devices. Various chapters advise on how to achieve patient confidentiality compliance for medical devices and their software, discuss legal issues surrounding device use in the hospital environment of care, the impact of device failures on patient safety, methods to advance skillsets for HTM professionals, and resources to assess digital technology. The authors bring forth relevant challenges and demonstrate how management can foster increased clinical and non-clinical collaboration to enhance patient outcomes and the bottom line by translating the regulatory impact on operational requirements.
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