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Webinar: In vitro skin sensitization testing: Ensuring conclusive results for challenging samples

November 20 @ 16:00 - 17:00

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.

Our 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.

You 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:

Agrochemical Formulations | Formulated Lubricant Products | Indirectly Acting Haptens | Metals | Natural Extracts | Polymers | UVCBs

Recorded webinar with live Q&A

This 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.

Key takeaways

  • NAMs and test strategies for skin sensitization testing of challenging samples.
  • The applicability domain of GARD®skin for challenging substances and its integration into Defined Approaches.
  • Case studies on Agrochemical Formulations, Formulated Lubricant Products, Indirectly Acting Haptens, Metals, Natural Extracts, Polymers, and UVCBs.


What are challenging /“difficult-to-test” substances?

In 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.

Read more about difficult-to-test substances.

Speaker

 

 

Details

Date:
November 20
Time:
16:00 - 17:00
Event Category:
Event Tags:
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Details

Date:
November 20
Time:
16:00 - 17:00
Event Category:
Event Tags:
, , , ,