USP 88 In-Vivo Cytotoxicity Testing
Learn what USP 88 cytotoxicity tests are available and which ones you will need to meet the regulatory requirements for your medical devices.
Learn what USP 88 cytotoxicity tests are available and which ones you will need to meet the regulatory requirements for your medical devices.
Learn what USP 87 cytotoxicity tests are available and which ones you will need to meet the regulatory requirements for medical products.
Learn about in-vitro vs. in-vivo medical device cytotoxicity assessments, and requirements of USP 87 and USP 88.
Learn what sensitization testing is and what sensitization tests are needed to meet regulatory requirements for medical devices.
Learn about cytotoxicity and physiochemical testing requirements for medical-grade plastics used in injectable products.
Learn about agar diffusion and elution tests for medical device cytotoxicity assessments and how to perform these kinds of tests.
Learn about agar diffusion and direct contact tests for medical device cytotoxicity assessments and how to perform these tests.
Learn about direct contact and elution tests for medical device cytotoxicity assessments and how to perform these tests.
Learn about the differences between cytotoxicity and microbiology testing, and when your medical device needs cytotoxicity and microbiology testing.
Learn about the differences between cytotoxicity and ethylene oxide (EO) residual testing for your medical devices or medical products.