Non-animal Vaginal Irritation Method Admitted into the US FDA Medical Devices Development Tool (MDDT)

18 Oct Non-animal Vaginal Irritation Method Admitted into the US FDA Medical Devices Development Tool (MDDT)

FDA’s recently launched Predictive Toxicology Roadmap calls for the optimization of non-animal methods for the safety evaluation of drugs, consumer products and medical devices. We have created an Industry Consortium comprised of manufacturers of personal lubricants/vaginal moisturizers and companies interested in the advancement of animal alternatives working collaboratively with stakeholders and the US FDA to develop an in vitro testing approach that could be used in place of the rabbit vaginal irritation (RVI) in pre-market submissions.

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