The safety assessment of Extractables and Leachables (E&Ls) is critical for product safety in sectors like pharmaceuticals and medical devices. In this presentation, we will provide an overview of E&L toxicological risk assessment, examining the potential structural classes of E&Ls, and addressing challenges associated with data-poor E&Ls. Specifically, we will discuss how in silico methods, including read-across, can facilitate the derivation of safety limits.
Presented by Candice Johnson, Product Manager & Frances Hall, Scientific Application Director
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