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Clinical Systems Engineering: New Challenges for Future Healthcare covers the critical issues relating to the risk management and design of new technologies in the healthcare sector. It is a comprehensive summary of the advances in clinical engineering over the past 40 years, presenting guidance on compliance and safety for hospitals and engineering teams.
This contributed book contains chapters from international experts, who provide their solutions, experiences, and the successful methodologies they have applied to solve common problems in the area of healthcare technology. Topics include
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Produktbeschreibung
Clinical Systems Engineering: New Challenges for Future Healthcare covers the critical issues relating to the risk management and design of new technologies in the healthcare sector. It is a comprehensive summary of the advances in clinical engineering over the past 40 years, presenting guidance on compliance and safety for hospitals and engineering teams.

This contributed book contains chapters from international experts, who provide their solutions, experiences, and the successful methodologies they have applied to solve common problems in the area of healthcare technology. Topics include compliance with the European Directive on Medical Devices 93/42/EEC, European Norms EN 60601-1-6, EN 62366, and the American Standards ANSI/AAMI HE75: 2009.

Content coverage includes decision support systems, clinical complex systems, and human factor engineering. Examples are fully supported with case studies, and global perspective is maintained throughout. This book isideal for clinical engineers, biomedical engineers, hospital administrators and medical technology manufacturers.

Presents clinical systems engineering in a way that will help users answer many questions relating to clinical systems engineering and its relationship to future healthcare needs Explains how to assess new healthcare technologies and what are the most critical issues in their management Provides information on how to carry out risk analysis for new technological systems or medical software Contains tactics on how to improve the quality and usability of medical devices
Autorenporträt
Dr Roberto Miniati received his M.Sc. in Biomedical Engineering in 2007 at the School of Engineering, University of Florence (Italy), and Ph.D. in 2012 within the international program on Risk Mitigation at the University of Florence (Italy) and TU Braunschweig (Germany). He has published over 100 scientific papers in refereed journals, international conference proceedings and book chapters. His main research fields include Healthcare Engineering, Health Technology Assessment (HTA) and Risk Management, Usability Engineering, Hospital Lean Manufacturing and Disaster Risk Reduction with focus in Health Emergency Planning and Vulnerability Assessment Methods.