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29 January 2024 | By Catherine Eckford (European Pharmaceutical Review)
Included in the revised ISO 10993-17 guideline are requirements for toxicological risk assessment of medical device constituents, such as extractables and leachables (E&L).
4 July 2023 | By Catherine Eckford (European Pharmaceutical Review)
Evaluation of bacterial endotoxin pyrogens is included in the International Organization for Standardization (ISO)’s new standard for microbiological methods.
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