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UID:30750-1683936000-1684022399@senzagen.com
SUMMARY:ISID 2023 Tokyo Satellite Meeting on Dermal Sensitization & Photoallergenicity
DESCRIPTION:This three-hour event kicks off with a welcome from Expert Panel for Fragrance Safety members Yoshiki Tokura\, MD\, PhD\, Donald V. Belsito\, MD\, and Magnus Bruce\, MD\, PhD\, and an introduction from RIFM’s President\, Anne Marie Api\, PhD\, ATS.\nSession \nDermal Sensitization & Photoallergenicity\n4:05-7:05 pm\, Saturday\, May 13\, 2023\nEminence Hall\, South Tower\, 5th Floor\, Keio Plaza Hotel\, Tokyo \n  \nSpeakers \nPresentations from international experts in toxicology and dermatology will include: \n\nMechanisms of Contact Dermatitis\, Kenji Kabashima\, MD\, PhD\, Kyoto Univ.\nRIFM Dermal Sensitization Program\, Isabelle Lee\, PhD\, RIFM\nOverview RIFM Photoallergy Research Program\, Gretchen Ritacco\, MS\, RIFM\nTrial for development of photo safety assessment system in Shiseido\, Shiho Oeda\, Shiseido\nRIFM-IIVS Photoallergy Research\, Allison Hilberer\, MS\, DABT\, IIVS\nRIFM-SenzaGen Photoallergy Research\, Andy Forreryd\, PhD\, SenzaGen
URL:https://senzagen.com/event/isid-2023-tokyo-satellite-meeting-on-dermal-sensitization-photoallergenicity/
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DTSTART;TZID=Europe/Stockholm:20230524T160000
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CREATED:20230510T075904Z
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UID:30647-1684944000-1684947600@senzagen.com
SUMMARY:Webinar: Using in vitro data in your CE marking submission of Medical Devices
DESCRIPTION:Join this free webinar to learn how you can avoid animal testing and accelerate time to market by using results from in vitro testing for the endpoints of cytotoxicity\, skin irritation and skin sensitization in your biological evaluation for CE-marking of your medical device in line with the EU Medical Device Regulation 2017/745\, the MDR.\n\nKey takeaways \n\nAn introduction to how in vitro testing can be used in the biological evaluation of your medical device with focus on cytotoxicity\, skin irritation and skin sensitization according to MDR.\nThe unique and broad applicability of the OECD approved GARD® assay for skin sensitization testing\, supporting polar and non-polar extraction vehicles as recommended in ISO 10993-12.\nSeveral application examples and a class IIa product CE marking case study supporting ethical test solutions and faster time to market.\nExpert advisory and support in compilation of regulatory documentation for instance gap analysis of ISO standards\, Biological Evaluation Plan (BEP) and Biological Evaluation Report (BER).\n\nSpeakers \n \n\nRegister here\n\n\nThe webinar will last around 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.
URL:https://senzagen.com/event/webinar-using-in-vitro-data-in-your-ce-marking-submission-of-medical-devices/
CATEGORIES:Webinar
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