VitroScreen has been a pioneer in developing and proposing pre-clinical experimental protocols on 3D reconstructed human tissue models: they are currently applied to demonstrate the mechanism of action of SBMD and they are relevant to comply with the safety and efficacy requirements of the EU MDR 2017/745. The seminar has the ambition to open a […]
Personal Care and Homecare Ingredients 2023 Expo & Shanghai Society of Toxicology Forum 15-17 February 2023 @The China Import and Export Fair Complex, Guangzhou, China Read More
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 […]
Meet us at this year's SOT Come meet us at our booth and join our hosted session to learn how the high performance and broad applicability of the GARDskin assay can be used to fill data gaps during regulatory testing and product development. Exhibitor-Hosted Session Posters 🎫 P117 | Joint poster with ExxonMobil Biomedical […]
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 […]
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. Session Dermal Sensitization & Photoallergenicity 4:05-7:05 pm, Saturday, May 13, 2023 Eminence Hall, South Tower, 5th […]
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. […]
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. […]
This two days hands-on training is hosted by acCELLerate. Skin sensitization is a complex systemic process and since several years, methods to replace animal tests have been validated and adopted by the OECD in this regard. These tests can be used as part of a weight-of-evidence or integrated using a Defined Approach (DA) to assess […]
Biocompatibility for Medical Devices Tuesday, 20 June 2023 12:00 - 12:30 The GARDskin Medical Device assay for assessing the skin sensitizing potential of medical devices: A case study on the use of in vitro data in the biological evaluation for CE marking according to MDR A proof-of-concept study using the GARDskin Medical Device assay to evaluate the […]
