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Standard and/or project Stage TC
Competence requirements for biorisk management advisors
50.20 ISO/TC 212
In vitro diagnostic test systems — Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methods
60.60 ISO/TC 212
Laboratory glassware — Disposable serological pipettes
90.60 ISO/TC 48
Plastics laboratory ware — Disposable serological pipettes
90.60 ISO/TC 48
Laboratory glassware — Disposable microhaematocrit capillary tubes
90.60 ISO/TC 48
Laboratory glassware — Desiccators
90.93 ISO/TC 48
Laboratory glassware — Petri dishes
95.99 ISO/TC 48
Laboratory glassware — Petri dishes
60.60 ISO/TC 48
Medical laboratories — Particular requirements for quality and competence
95.99 ISO/TC 212
Medical laboratories — Particular requirements for quality and competence
95.99 ISO/TC 212
Medical laboratories — Requirements for quality and competence
95.99 ISO/TC 212
Medical laboratories — Requirements for quality and competence
60.60 ISO/TC 212
Medical laboratories — Requirements for safety
95.99 ISO/TC 212
Medical laboratories — Requirements for safety
60.60 ISO/TC 212
Medical laboratories — Reagents for staining biological material — Guidance for users
90.93 ISO/TC 212
In 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 definitions
95.99 ISO/TC 212
In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens — Laboratory quality practice guide
60.60 ISO/TC 212
Requirements for the collection and transport of samples for medical laboratory examinations
60.60 ISO/TC 212
Medical laboratories — Requirements for collection, transport, receipt, and handling of samples
95.99 ISO/TC 212
Medical laboratories — Practical guidance for the estimation of measurement uncertainty
90.93 ISO/TC 212
Medical laboratories — Application of risk management to medical laboratories
90.92 ISO/TC 212
Medical laboratories — Reduction of error through risk management and continual improvement
95.99 ISO/TC 212
Medical laboratories — Reduction of error through risk management and continual improvement — Technical Corrigendum 1
95.99 ISO/TC 212
Guidance for supervisors and operators of point-of-care testing (POCT) devices
90.92 ISO/TC 212
Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipment
50.20 ISO/TC 212
Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003
95.99 ISO/TC 212
Point-of-care testing (POCT) — Requirements for quality and competence
95.99 ISO/TC 212
Point-of-care testing (POCT) — Requirements for quality and competence
95.99 ISO/TC 212
Basic semen examination — Specification and test methods
60.60 ISO/TC 212
Medical laboratories — Guidance on application of ISO 15189 in anatomic pathology
50.20 ISO/TC 212
Plastics laboratory ware — Single-use Petri dishes for microbiological procedures
90.93 ISO/TC 48
Biorisk management for laboratories and other related organisations
60.60 ISO/TC 212
Biorisk management for laboratories and other related organisations — Amendment 1: Climate action changes
60.60 ISO/TC 212

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