In the past 15 years, ISO 10993-18 has become a guiding light for professionals at every stage in the medical device manufacturing and supply chain, by helping them assess the chemical risk associated with their products. Our latest whitepaper discusses the most recent revisions to ISO 10993-18, which focus on how to account for variability in quantitation practices.
If you have any questions that aren’t answered in the whitepaper, feel free to contact a member of the Jordi Labs team today. Our experienced team of P.hD chemists has significant experience in regulatory testing according to ISO standards, and would be happy to help.
