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Biological evaluation of medical devices — Part 23: Tests for irritation - Amendment 1: Biological evaluation of medical devices — Part 23: Tests for irritation — Amendment 1
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18/11/2024
Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipment
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for professional use
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling). Part 5: In vitro diagnostic instruments for self-testing
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Terms, definitions, and general requirements
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for self-testing
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for professional use
Medical laboratories. Guidance on application of ISO 15189 in anatomic pathology
Competence requirements for biorisk management advisors