ISO 10993-17:2023, what’s new

The purpose of this webinar is to provide participants with a comprehensive understanding of Toxicological Risk Assessment (TRA) for medical devices, with a particular emphasis on the new ISO 10993-17:2023. TRA is a critical aspect of ensuring the safety and biocompatibility of medical devices.

This webinar aims to equip attendees with the knowledge and skills necessary to conduct effective TRA in compliance with international standards and regulations.

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