Toxikon’s Microbiology Department effectively collaborates with clients to develop customized study protocols that meet your specific requirements. Our staff of experienced microbiologists apply their technical expertise when conducting each study to generate timely, quality data to your program’s requirements.
Microbiological characterization of medical devices typically accompany regulatory submissions and bioburden, endotoxin, and tests for sterility are common requirements. Similarly, reusable medical devices require validation testing to confirm the procedures used to clean, disinfect, and/or sterilize a device between use are effective.
Testing Capabilities Include: