Filtrar :
Norma o proyecto | Etapa | 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
|
60.60 | 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
|
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
|
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
|
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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