Webinar: How to use in vitro assays in your biological evaluation

In this webinar, our Medical Device and ISO expert Dr Rose-Marie Jenvert will tell you more about how you can use in vitro methods for the biological evaluation of medical devices, now offered at our GLP-certified laboratories. She will also introduce you to our expanded medical device offering and how we can help you to […]

Webinar: Safety and Efficacy Evaluation of Cosmetic Products and Ingredients

How to integrate innovative in vitro test methods In this joint webinar, we will present an overview of innovative in vitro methods and how to integrate them into the evaluation of safety and efficacy of cosmetic products and ingredients. The webinar will start with a recorded presentation followed by a live Q&A session. If you […]

Webinar: Overcoming challenges in skin sensitization testing with GARDskin OECD TG 442E

Free webinar on Feb 22, 2023 | 4pm CET | 10am EST Together with guest speakers Dr Marco Corvaro, Technical Team Leader, Regulatory Toxicology at Corteva Agriscience and Gretchen Ritacco, Principal Scientist at the Research Institute for Fragrance Materials (RIFM), we will discuss the challenges in skin sensitization testing and present new scientific data on […]

SOT2023 Recap Webinar

In case you missed SenzaGen’s Scientific Session at this year’s SOT, here is a new opportunity! Together with guest speakers from ExxonMobil Biomedical Sciences Inc. and Research Institute for Fragrance Materials, Inc. (RIFM), SenzaGen’s Andy Forreryd, PhD will present the latest GARD® data on quantitative risk assessment and regulatory testing of skin sensitizers, and the […]

Webinar: Using in vitro data in your CE marking submission of Medical Devices

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. […]

Webinar: Time for a Change: Evidence-Based Approaches for the Biological Safety Assessment of Medical Devices

Join this free webinar where Ron Brown, toxicologist and former FDA risk assessor, will outline the need for a new and more agile approach for the biological safety assessment of medical devices. This presentation will identify the limitations associated with the current approach, which largely relies on animal-based tests that may have questionable clinical relevance. […]

Webinar: Safety of acrylate monomers, metals, and other materials used in medical device development

Join our upcoming free webinar to explore the effective utilization of in vitro methods for safety assessment of materials during product development of Medical Devices. We will discuss recent advancements in in vitro methods for assessing the endpoints of skin irritation and skin sensitization. Learn how to integrate these assessments into your product development process […]

Webinar: Spotlight on Difficult-to-Test samples

Join our upcoming webinar to explore the recent advancement in GARD® for Skin Sensitization assessment, with a specific focus 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 […]

Webinar: Advancing NAMs for Skin Sensitization Testing

Spotlight on Applicability Domain, Quantitative Potency Assessment and Medical Devices In case you missed SenzaGen’s poster presentations and scientific session at this year’s SOT, we are pleased to offer you a new opportunity to participate on April 23, 2024! In this webinar Dr Andy Forreryd, SenzaGen's in vitro toxicology expert, will summarize the latest GARD data from industry collaborations: […]