Clinical Engineering A Handbook for Clinical and Biomedical Engineers
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Form:Einzelkauf Download
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Sprache:Englisch
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eBook Format:ePUB 3
- ePUB 3 131,00 € ausgewählt
- ePUB 92,95 €
131,00 €
inkl. gesetzl. MwSt.Beschreibung
Produktdetails
Format
ePUB 3
Kopierschutz
Nein
Family Sharing
Nein
Text-to-Speech
Ja
Erscheinungsdatum
01.12.2019
Herausgeber
Azzam Taktak + weitereVerlag
Elsevier Science & Techn.Seitenzahl
552 (Printausgabe)
Auflage
2. Auflage
Sprache
Englisch
EAN
9780081026953
Clinical Engineering: A Handbook for Clinical and Biomedical Engineers, Second Edition, helps professionals and students in clinical engineering successfully deploy medical technologies. The book provides a broad reference to the core elements of the subject, drawing from a range of experienced authors. In addition to engineering skills, clinical engineers must be able to work with both patients and a range of professional staff, including technicians, clinicians and equipment manufacturers. This book will not only help users keep up-to-date on the fast-moving scientific and medical research in the field, but also help them develop laboratory, design, workshop and management skills.
The updated edition features the latest fundamentals of medical technology integration, patient safety, risk assessment and assistive technology.
- Provides engineers in core medical disciplines and related fields with the skills and knowledge to successfully collaborate on the development of medical devices, via approved procedures and standards
- Covers US and EU standards (FDA and MDD, respectively, plus related ISO requirements)
- Includes information that is backed up with real-life clinical examples, case studies, and separate tutorials for training and class use
- Completely updated to include new standards and regulations, as well as new case studies and illustrations
The updated edition features the latest fundamentals of medical technology integration, patient safety, risk assessment and assistive technology.
- Provides engineers in core medical disciplines and related fields with the skills and knowledge to successfully collaborate on the development of medical devices, via approved procedures and standards
- Covers US and EU standards (FDA and MDD, respectively, plus related ISO requirements)
- Includes information that is backed up with real-life clinical examples, case studies, and separate tutorials for training and class use
- Completely updated to include new standards and regulations, as well as new case studies and illustrations
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