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Dealing with Out of Domain (Q)SAR Predictions for ICH M7: A Regulatory and Industrial Perspective

Kruhlak NL; Kenyon MO;

Presented by Dr Naomi Kruhlak, Lead for the Division of Applied Regulatory Science's Chemical Informatics Program at FDA’s Center for Drug Evaluation and Research (CDER), and Michelle Kenyon, Senior Principal Scientist in the Genetic Toxicology Department at Pfizer and Chair of the Board of Directors of the Genetic Toxicology Association.


This was presented as part of Lhasa Limited's 2017 series of vICGMs.


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