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Paolo Pescio

Eurofins Medical Device Testing

Paolo is Senior Consultant at Eurofins Medical Device Testing Italy. He’s a European Registered Toxicologist (ERT), HAS consultant and has more than 15 years of experience with medical devices. Toxicological evaluation and risk assessment, Biological evaluation of medical devices and Integrated Testing Strategies are his specialties.

Learn more about Eurofins Medical Device Testing, visit their website!


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Session:

Chemical Characterisation: a prerequisite for the biological evaluation

Location Einstein C Room Start / end time 4:30 pm to 5:15 pm

The new ISO 10993-18:2020 (Biological evaluation of medical devices – Part 18: Chemical characterization of medical device materials within a risk management process) was finally published at the beginning of the year.
The focus of chemical characterization will not only be to evaluate the raw materials but also to take into account the presence of any impurities or residues associated with the manufacturing and sterilization process that may impact medical devices biocompatibility.
Chemical characterization becomes a key factor in the assessment of the biological evaluation since obtained data are fundamental to correctly set the biological risk assessment of medical devices and also to plan how to evaluate biological effects relevant to the device.

This workshop will provide an up-to-date overview on normative changes of the new ISO 10993-18 in relation with the biological evaluation of devices and planning for future testing.