Mitigating Biocompatibility Risks in Medical Device Manufacturing

The medical devices and surgical tools used in the medical industry every day are subject to strict testing standards dictated by the FDA and other regulatory bodies using ASTM and ISO methodologies. Cleanliness testing ensures that materials used in medical implants – as well as surgical, diagnostic, and therapeutic tools – won’t have adverse toxic effects when utilized for patient treatments.

We’ve put together an informative eBook with everything you need to know about medical device biocompatibility risks, including:

  • Standards for Medical Cleanliness
  • Cytotoxic Reactions
  • Testing Methods for Biocompatibility
  • And much more...

 



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