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Creating Toxicological Risk Assessments for 
Medical Devices
There has been a substantial regulatory emphasis on obtaining chemical information about a medical device. But how does one take that information and translate it to patient safety? This is where ISO 10993-17 and toxicological analysis come into play. In this whitepaper, we will outline the process by which these standards are used to determine the toxicological risk associated with chemicals originating from a medical device.
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