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Published by Elsevier Science Ltd, 2016
ISBN 10: 012804179X ISBN 13: 9780128041796
Language: English
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Add to basketPaperback. Condition: Brand New. 380 pages. 9.00x7.25x0.75 inches. In Stock.
Published by Elsevier Science Publishing Co Inc, 2016
ISBN 10: 012804179X ISBN 13: 9780128041796
Language: English
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Add to basketPaperback / softback. Condition: New. New copy - Usually dispatched within 4 working days. 790.
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
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Add to basketCondition: New. Covers compliance with FDA and CE regulations, plus EU directives for service and maintenance of medical devices Provides operational and clinical practice recommendations in regard to regulatory changes for risk management Discus.
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Published by Elsevier Science & Technology Sep 2016, 2016
ISBN 10: 012804179X ISBN 13: 9780128041796
Language: English
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Add to basketTaschenbuch. Condition: Neu. Neuware - 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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