DIN EN ISO 10993-1 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system
DIN EN ISO 10993-5 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity.
DIN EN ISO 10993-12 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials.
USP 38 <87> Biological reactivity tests, in vitro.
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