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Reviews recent advances in the understanding of solid and liquid biomaterials and of viscoelastic solids and liquids. Includes discussions of the single material characteristic in biological materials of interest for structural uses (wood), and for nutritional uses (gels and gums) and medical purposes (artificial skins and membranes). Twenty-six chapters provide the reader with a perspective on the current state of knowledge of biomaterial science as it affects medical, nutritional, and structural fields of science.

Biomedical materials - Congresses. --- Viscoelasticity - Congresses. --- Biopolymers - Congresses. --- Biomedical materials --- Biopolymers --- Viscoelasticity --- Congresses.

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Biomedical materials --- Surfaces --- Congresses. --- Congresses --- Biomedical materials - Surfaces - Congresses. --- Oral medicine --- Biocompatible Materials --- Dental Implants --- Man --- Oral region --- Implants --- Polyurethanen. (Congres) --- Polymères / en médecine. (Congrès) --- Polyuréthane. (Congrès) --- Polymeren / in de geneeskunde. (Congres)

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612.76 --- 617 --- #TWER:BIOM --- Locomotie. Beweging. Lichaamsmechanica. Biomedische ingenieurstechnieken --- Orthopedie. Oftalmologie --- Biomedical materials --- Congresses --- Biomedical engineering

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Biomedical materials --- Terminology --- Congresses --- -#TWER:BIOM --- Biocompatible materials --- Biomaterials --- Medical materials --- Medicine --- Biomedical engineering --- Materials --- Biocompatibility --- Prosthesis --- -Congresses --- #TWER:BIOM --- Terminology&delete& --- Matériaux biomédicaux. Terminologie anglaise. (Congrès) --- Biomedische materialen. Termen (Engelse). (Congres) --- Bioartificial materials --- Hemocompatible materials --- Biomaterials (Biomedical materials) --- Biomedical materials - Terminology - Congresses

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Medical devices and equipment are a vital component of patient care. From a simple tongue depressor to a sophisticated haemodialysis machine, medical devices are needed at every level of the health service. Yet many health services continue to lack information and financial resources to acquire the devices they really need, i.e. those that will address the specific disease burden in their country. Effective implementation of a National Regulatory Authority is a first step towards the cost-effective management of medical devices that meet international quality and safety standards, throughout their entire life span, from conception to disposal. This publication offers countries a framework within which they can plan - or improve - their regulatory system for medical devices. Governments are particularly encouraged to take advantage of the extensive work undertaken over the last ten years by national and regional bodies to harmonize regulations on medical devices. Countries can also adopt the device approvals of the advanced regulatory systems. These two approaches alone can enable national health authorities to redirect scarce resources towards locally-assessed needs, such as vendor and device registration, training, surveillance and information exchange systems on medical devices in use.

Gestion des risques --- Gestion du risque --- Kwaliteitscontrole --- Maîtrise des risques --- Quality control --- Qualité [Contrôle de la ] --- Risicobeheer --- Risk management --- Risque -- Gestion --- Risques -- Gestion --- Equipment and supplies --- Legislation --- Standards --- Medical instruments and apparatus --- Biomedical materials --- Biocompatible materials --- Biomaterials --- Medical materials --- Medicine --- Biomedical engineering --- Materials --- Biocompatibility --- Prosthesis --- Standards. --- Bioartificial materials --- Hemocompatible materials --- Biomaterials (Biomedical materials)