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.
ISO 10993-17:2023, what’s new
FREE ONLINE WEBINAR: To continue supporting our customers' needs this webinar is dedicated to manufacturers only. To allow all interested companies attend, maximum two delegates form the same company will be admitted. Due to the type of event and limited audience capacity, participation of companies not included in this category will not be accepted. Attendance will be confirmed from the event's organizers.
DATE: November 30, 2023 | 3.00 PM - 4.00 PM CET
OFFICIAL LANGUAGE: English
SUBMISSION LINK: https://attendee.gotowebinar.com/register/1340397467102897496
ATTENDEES CAPACITY: 500 delegates
The event will be hosted within Go ToWebinar platform. Your registration request for this webinar will be submitted to the organizer for approval. You will receive information via email regarding your registration status.
Speaker
European Registered Toxicologist with a MSc in Applied Toxicology and Biomedical Engineering, Paolo has over 15 years of experience in biological evaluation of medical devices and toxicological risk assessment for pharmaceutical products. He is Senior Scientific Director at Eurofins Medical Device Testing Europe, member of ISO TC 194 and CEN TC 206 and adjunct professor at the University of Milan and Fondazione Alma Mater of Bologna. He is a former Healthcare Engineering HAS consultant for EU Commission.