Filter :
Standard and/or project | Stage | TC |
---|---|---|
Competence requirements for biorisk management advisors |
60.00 | 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 |
60.00 | 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 |
60.00 | 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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