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X-WR-CALDESC:Events for SenzaGen
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DTSTART:20260329T010000
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DTSTART:20261025T010000
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DTSTART;TZID=Europe/Stockholm:20261006T160000
DTEND;TZID=Europe/Stockholm:20261006T170000
DTSTAMP:20261029T062425
CREATED:20260923T132327Z
LAST-MODIFIED:20260924T074811Z
UID:37439-1791302400-1791306000@senzagen.com
SUMMARY:Webinar: In vitro skin sensitization potency assessment - Part 3
DESCRIPTION:Expert roundtable: How do we assess skin sensitization potency of Complex Mixtures?\nIndustry and scientific perspectives on current challenges\, emerging approaches and new data on Essential Oils\nHow can reliable skin sensitization potency estimates be generated for Natural Complex Substances and other complex mixtures using New Approach Methodologies (NAMs)? \nIn this webinar\, Joe Dawson\, Product Safety Manager at dōTERRA\, will present key findings from a recently published study comparing different approaches to quantitative potency assessment of Essential Oils. \nThe presentation will be followed by a live expert roundtable featuring speakers from dōTERRA\, the Research Institute for Fragrance Materials (RIFM)\, and SenzaGen. Together\, the panel will explore current challenges\, practical applications\, and future directions for skin sensitization potency assessment of complex mixtures. \nFor those who missed our EUROTOX session\, this webinar also offers an opportunity to hear the scientific rationale and key findings behind the newly published study. \nThe webinar presentations will last around 25 minutes\, followed by a 35-minutes live Q&A and expert roundtable discussion. If you cannot attend the live event\, register now to get access to the recording 🎧. \nWhat is your biggest challenge in skin sensitization potency assessment? Submit your question in the registration form and help shape the expert roundtable discussion. Selected questions and topics will be featured during the live session. \n  \n \nKey takeaways\n\nInsights from a newly published study comparing GARD® skin Dose-Response\, component-based prediction model\, and historical LLNA data for Essential Oils.\nCurrent challenges and opportunities in quantitative skin sensitization potency assessment of Complex Mixtures.\nExpert perspectives on practical applications\, challenges\, and future directions in NAM-based potency assessment.\n\nSpeakers\n \nAndy Forreryd\, PhD\nScientific Liaison Manager @ SenzaGen \n\nCo-developer of the GARD®skin assay (OECD TG 442E).\nMember of the ISO/TC 194/WG 8 on irritation and sensitization.\nMember of OECD expert group on respiratory sensitization.\n\n\nIntroduction to skin sensitization potency assessment and the single assay-based method GARD® skin Dose-Response. \n\n  \n \nJoe Dawson\nProduct Safety Manager @ dōTERRA\n \n\n12 years of experience as a research scientist in the food and cosmetics industries\nExpertise in product safety and scientific evaluation of consumer products\nB.Sc. in Molecular Biology\, University of Utah\, M.S. in Biomedical Informatics at the University of Utah School of Medicine (ongoing).\n\nA comparative analysis of test methods for predicting dermal sensitization potency in Essential Oils. \n  \n \nIsabelle Lee\, PhD\nManager of Human Health Science & Strategy @ RIFM\n \n\nLeads human health science and strategy\, advancing NAMs for ingredient safety.\nHead of skin sensitization team\, overseeing safety assessments and research programs.\nExpert in consumer product ingredient evaluation with a PhD in Pharmacology (UPenn).\n\n 
URL:https://senzagen.com/event/2026-webinar-in-vitro-skin-sensitization-potency-assessment-part-3/
CATEGORIES:Webinar
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DTSTART;TZID=Europe/Stockholm:20261028T160000
DTEND;TZID=Europe/Stockholm:20261028T170000
DTSTAMP:20261029T062425
CREATED:20261009T120435Z
LAST-MODIFIED:20261022T093939Z
UID:37548-1793203200-1793206800@senzagen.com
SUMMARY:Webinar: Advancing Medical Device Biocompatibility testing with NAMs
DESCRIPTION:Regulatory updates\, industry case studies\, and newly published evidence for wearable devices\nCan the “Big Three” be addressed using non-animal methods? Scientifically validated in vitro approaches are available to assess cytotoxicity\, skin irritation and skin sensitization\, supporting more predictive and human-relevant biocompatibility testing. As the regulatory landscape continues to evolve\, medical device manufacturers face growing opportunities to incorporate these methods into biocompatibility assessments and regulatory submissions. \nJoin us for a webinar exploring the latest developments within the ISO 10993 framework and how New Approach Methodologies (NAMs) are being applied in practice. We are also pleased to welcome Florian Gerdts\, Team Lead Process Development at Element 22\, who will present a case study on metallic 3D-printing materials. \nThrough regulatory perspectives and industry case studies\, our speakers will discuss how in vitro methods can support decision-making from early material screening to CE-marking submissions. \nJust published: We will also present findings from a newly published peer-reviewed study on wearable devices\, providing new evidence for the use of GARD® assays in assessing both constituents and finished-product leachables. \nBuild readiness\n• Develop your NAM database\n• Gain testing experience\n• Strengthen weight-of-evidence assessments \n \nThe webinar will last around 45 minutes\, followed by a live Q&A. If you cannot attend the live event\, register anyway to receive the recording. \nKey takeaways\n\nRegulatory insights: Stay informed on the latest developments in ISO 10993-5\, ISO 10993-23 and ISO 10993-10\, and the growing role of in vitro methods. \nGARD® advancements: Learn how GARD® supports both skin sensitization hazard and quantitative potency assessment of extractable medical devices and solid materials in polar and non-polar vehicles. \nIndustry application: Discover how NAMs are used as weight-of-evidence in CE-marking submissions\, testing of 3D-printed oral devices\, metallic 3D-printing materials\, and early-stage material screening.\nFeatured publication: “Assessing the skin sensitizing potential of constituents and leachables from wearable devices using GARD®” by Persaud et al. (Apple\, SenzaGen). Learn how the study applies GARD® assays to both wearable device constituents and finished-product leachables.\n\n\nSpeaker\n \nAndy Forreryd\, PhD\nScientific Liaison Manager @ SenzaGen \n\nCo-developer of the GARD®skin assay (OECD TG 442E).\nMember of the ISO/TC 194/WG 8 on irritation and sensitization.\nMember of OECD expert group on respiratory sensitization.\n\n  \n \nFlorian Gerdts\nTeam Lead Process Development @ Element 22 GmbH \n\nMaster of Materials Science and Engineering\, CAU Kiel\nTitanium Powder Metallurgy Expert\n> 14 years of experience in Titanium Pulver Metallurgy.\n\n  \n \n  \n\n 
URL:https://senzagen.com/event/webinar-medical-device-biocompatibility-testing-2026/
CATEGORIES:Webinar
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