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DTSTART;TZID=Europe/Stockholm:20241120T160000
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SUMMARY:Webinar: In vitro skin sensitization testing: Ensuring conclusive results for challenging samples
DESCRIPTION:Join us for a special re-run of our popular GARD® webinar to explore the recent advancement in Skin Sensitization testing\, focusing on substances that fall outside the applicability domains of the conventional in vitro assays in the OECD Test Guidelines. \nOur skin sensitization experts will address challenges posed by various “Difficult-to-Test” substances\, discussing the applicability domain of key event-based NAMs and existing test strategies. \nYou will learn about the broad applicability of GARD®skin (OECD TG442E) as we review scientific data on challenging substances and exciting projects done in collaboration with industry partners: \nAgrochemical Formulations | Formulated Lubricant Products | Indirectly Acting Haptens | Metals | Natural Extracts | Polymers | UVCBs \nRecorded webinar with live Q&A\nThis recorded webinar will last approximately 45 minutes\, followed by a live Q&A. If you cannot attend the live event\, make sure to register to get access to the recording.  \nKey takeaways\n\nNAMs and test strategies for skin sensitization testing of challenging samples.\nThe applicability domain of GARD®skin for challenging substances and its integration into Defined Approaches.\nCase studies on Agrochemical Formulations\, Formulated Lubricant Products\, Indirectly Acting Haptens\, Metals\, Natural Extracts\, Polymers\, and UVCBs.\n\nWhat are challenging /“difficult-to-test” substances?\nIn the context of skin sensitization testing\, certain groups of chemicals are considered difficult to test using conventional cell-based methods. Examples of commonly recognised “difficult-to-test” samples include indirectly acting haptens\, complex mixtures\, and substances with low water solubility. \nRead more about difficult-to-test substances. \nSpeaker\n \n  \n \n 
URL:https://senzagen.com/event/webinar-spotlight-on-challenging-samples/
CATEGORIES:Webinar
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