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ISO/TR 15499:2016WithdrawnBiological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management processISO/TR 15499:2012WithdrawnBiological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management processISO 16256:2012WithdrawnClinical laboratory testing and in vitro diagnostic test systems — Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseasesISO 17511:2003WithdrawnIn vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values assigned to calibrators and control materialsISO 17593:2007WithdrawnClinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapyISO/TS 17822-1:2014WithdrawnIn vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens — Part 1: General requirements, terms and definitionsISO/TR 18112:2006WithdrawnClinical laboratory testing and in vitro diagnostic test systems — In vitro diagnostic medical devices for professional use — Summary of regulatory requirements for information supplied by the manufacturerISO 18113-1:2009WithdrawnIn vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirementsISO 18113-2:2009WithdrawnIn vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional useISO 18113-3:2009WithdrawnIn vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional useISO 18113-4:2009WithdrawnIn vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testingISO 18113-5:2009WithdrawnIn vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testingISO 18153:2003WithdrawnIn vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values for catalytic concentration of enzymes assigned calibrators and control materialsISO/PAS 18873:1999WithdrawnInternational protocol for doping controlISO 19001:2002WithdrawnIn vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyISO/TS 20658:2017WithdrawnMedical laboratories — Requirements for collection, transport, receipt, and handling of samplesISO 20776-2:2007WithdrawnClinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 2: Evaluation of performance of antimicrobial susceptibility test devicesISO 20776-1:2006WithdrawnClinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseasesISO/TS 20993:2006WithdrawnBiological evaluation of medical devices — Guidance on a risk-management processISO 22367:2020WithdrawnMedical laboratories — Application of risk management to medical laboratoriesISO/TS 22367:2008WithdrawnMedical laboratories — Reduction of error through risk management and continual improvementISO 22442-1:2015WithdrawnMedical devices utilizing animal tissues and their derivatives — Part 1: Application of risk managementISO 22442-2:2015WithdrawnMedical devices utilizing animal tissues and their derivatives — Part 2: Controls on sourcing, collection and handlingISO 22442-1:2007WithdrawnMedical devices utilizing animal tissues and their derivatives — Part 1: Application of risk managementISO 22442-2:2007WithdrawnMedical devices utilizing animal tissues and their derivatives — Part 2: Controls on sourcing, collection and handling