Enabling Innovation in Medicine and Healthcare

Biocompatibility

Zymetrix conducts in-vitro studies to support the requirements of ISO 10993:  Biological Evaluation of Medical Devices for regulatory submissions.  Our specific emphasis in this area is on biomaterials and Tissue Engineered Medical Products (TEMPs)

All of our work in characterizing biomaterials is conducted within a GLP compliant Biosafety Level 2 laboratory.