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Regulatory Affairs for Biomaterials and Medical Devices
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All biomaterials and medical devices are subject to a long list of regulatory practises and policies which must be adhered to in order to receive clearance. Thi
Biomaterials, Medical Devices and Tissue Engineering: An Integrated Approach
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are then selected and must meet the general 'biocompatibility' require ments. Prototypes are built and tested to include biocompatibility evalua tions based on
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The effective sterilisation of any material or device to be implanted in or used in close contact with the human body is essential for the elimination of harmfu
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Metallic Biomaterials Processing and Medical Device Manufacturing details the principles and practices of the technologies used in biomaterials processing and m