Every medical device needs to have proven biocompatibility to protect users from potential biological risks arising from its intended use. In particular, cytotoxicity must be evaluated for every medical device, regardless of its classification. Cytotoxicity testing using in vitro cell cultures is common and offers high sensitivity and low cost. But too much sensitivity can result in failures. What to do? Attend this webinar for a step-by-step guide to help you investigate and assess in vitro cytotoxicity failures – and determine appropriate solutions.
Dates and locations:
Available On Demand Until 12/1/2024