Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)
Aseptic processing of health care products - Part 4: Clean-in-place technologies (ISO 13408-4:2005)
Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)
Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012)
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009)
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003)
In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2018)
In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
Single-use containers for human venous blood specimen collection
53,361 distinct reference strings indexed from official source snapshots accessed on 19 October 2026. Includes earlier editions. The index and publisher collections have different coverage. See sources and coverage.