For assessment of skin sensitization, the GARD™-technology will be introduced and the speakers will discuss how it can be used as a part of a biological evaluation.
TORONTO (PRWEB)
September 28, 2021
In this webinar, the speakers will discuss the uses of in vitro assays as a part of the risk assessment and biological evaluation for the following endpoints: cytotoxicity, skin irritation and skin sensitization.
The presentation will introduce biological evaluation and biocompatibility testing of medical devices, with focus on in vitro assays for skin irritation and skin sensitization now implemented in the ISO 10993-23:2021 and ISO/FDIS 10993-10:2021. For assessment of skin sensitization, the GARD™-technology will be introduced and the speakers will discuss how it can be used as a part of a biological evaluation.
The webinar will conclude with customer cases where in vitro assays, including GARDskin Medical Device assay and GARDskin Dose-Response, have been successfully utilized for risk assessment as part of the biological evaluation and for risk-based decision-making in compliance with the principles of the 3Rs throughout the product life cycle.
Join expert speakers from SenzaGen AB, Rose-Marie Jenvert, PhD, Product Manager and Tim Lindberg, PhD, Key Account Manager in a live webinar on Wednesday, October 13, 2021 at 10am EDT (3pm BST/UK).
For more information, or to register for this event, visit Safer Medical Devices – In Vitro Assays As Part of a Biological Evaluation.
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