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            | Standard and/or project | Stage | TC | 
|---|---|---|
| 
                     Competence requirements for biorisk management advisors 
                     | 
                  60.60 | 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 
                     | 
                  90.20 | ISO/TC 212 | 
| 
                     Laboratory glassware — Disposable serological pipettes 
                     | 
                  90.93 | ISO/TC 48/SC 8 | 
| 
                     Plastics laboratory ware — Disposable serological pipettes 
                     | 
                  90.93 | ISO/TC 48/SC 8 | 
| 
                     Laboratory glassware — Disposable microhaematocrit capillary tubes 
                     | 
                  90.60 | ISO/TC 48/SC 7 | 
| 
                     Laboratory glassware — Desiccators 
                     | 
                  90.93 | ISO/TC 48/SC 7 | 
| 
                     Laboratory glassware — Petri dishes 
                     | 
                  95.99 | ISO/TC 48 | 
| 
                     Laboratory glassware — Petri dishes 
                     | 
                  60.60 | ISO/TC 48/SC 7 | 
| 
                     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 
                     | 
                  90.20 | 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 | 
| 
                     Medical laboratories — Application of risk management to medical laboratories 
                     | 
                  40.20 | ISO/TC 212 | 
| 
                     Laboratory design — Vocabulary 
                     | 
                  40.20 | ISO/TC 336 | 
| 
                     Guidance for supervisors and operators of point-of-care testing (POCT) devices 
                     | 
                  95.99 | ISO/TC 212 | 
| 
                     Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipment 
                     | 
                  60.60 | 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 
                     | 
                  60.60 | ISO/TC 212 | 
| 
                     Plastics laboratory ware —  Single-use Petri dishes for microbiological procedures 
                     | 
                  90.93 | ISO/TC 48/SC 7 | 
| 
                     Biorisk management for laboratories and other related organisations 
                     | 
                  90.60 | 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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