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GSO ISO 16256:2024
ISO 16256:2021
Gulf Standard
Clinical laboratory testing and in vitro diagnostic test systems — Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
GSO ISO 18113-4:2024
ISO 18113-4:2022
Gulf Standard
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
GSO ISO 18113-3:2024
ISO 18113-3:2022
Gulf Standard
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
GSO ISO 6717:2024
ISO 6717:2021
Gulf Standard
In vitro diagnostic medical devices — Single-use containers for the collection of specimens from humans other than blood
GSO ISO 18113-5:2024
ISO 18113-5:2022
Gulf Standard
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
GSO ISO 17511:2024
ISO 17511:2020
Gulf Standard
In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
GSO ISO 21474-2:2024
ISO 21474-2:2022
Gulf Standard
In vitro diagnostic medical devices
— Multiplex molecular testing for nucleic acids
— Part 2: Validation and verification
GSO ISO 21474-1:2024
ISO 21474-1:2020
Gulf Standard
In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 1: Terminology and general requirements for nucleic acid quality evaluation
GSO ISO 20186-1:2024
ISO 20186-1:2019
Gulf Standard
Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA
GSO ISO 18113-1:2024
ISO 18113-1:2022
Gulf Standard
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
GSO ISO 18113-2:2024
ISO 18113-2:2022
Gulf Standard
In vitro diagnostic medical devices
— Information supplied by the manufacturer (labelling)
— Part 2: In vitro diagnostic reagents for professional use
GSO ISO 20184-3:2023
ISO 20184-3:2021
Gulf Standard
Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 3: Isolated DNA