Biocompatibility and Performance of Medical Devices 2012
DOI: 10.1533/9780857096456.2.95
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Allowable limits for toxic leachables: practical use of ISO 10993-17 standard * *The recommendations offered in this chapter should not be construed as guidance from the US Food and Drug Administration (FDA). The mention of commercial products, their sources or their use in connection with material reported herein is not to be construed as either an actual or implied endorsement of such products by the Department of Health and Human Services.

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“…Regenerative medicine and specifically tissue engineering have grown exponentially in the number of publications, with the latter being one of the advances in biomedicine with greater impact [ 1 , 2 ]. This growth is due to the creation of new processing protocols that improve the quality of biomaterials [ 3 ].…”
Section: Introductionmentioning
confidence: 99%
“…Regenerative medicine and specifically tissue engineering have grown exponentially in the number of publications, with the latter being one of the advances in biomedicine with greater impact [ 1 , 2 ]. This growth is due to the creation of new processing protocols that improve the quality of biomaterials [ 3 ].…”
Section: Introductionmentioning
confidence: 99%