Document Center List of Standards on Laboratory Medicine In General
ICS Code 11.100.01
Return to ICS Index.Up to Level 2:
The following documents are a part of this series:
ASTM:
- ASTM-D7372 - Standard Guide for Analysis and Interpretation of Proficiency Test Program Results
- ASTM-E1415 - Standard Guide for Conducting Static Toxicity Tests With
Lemna gibba G3 - ASTM-E2549 - Standard Practice for Validation of Seized-Drug Analytical Methods (Withdrawn 2023)
- ASTM-E3148 - Standard Guide for Postmortem Facial Image Capture
- ASTM-F3206 - Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies
BSI:
- BS-EN-ISO-15189 - Medical laboratories. Requirements for quality and competence
- BS-EN-ISO-22367 - Medical laboratories. Application of risk management to medical laboratories
- BS-EN-ISO-22870 - Point-of-care testing (POCT). Requirements for quality and competence
- BS-EN-ISO-22870-TC - Tracked Changes. Point-of-care testing (POCT). Requirements for quality and competence
- BS-EN-ISO-23162 - Basic semen examination. Specification and test methods
- BS-ISO-15190-TC - Tracked Changes. Medical laboratories. Requirements for safety
- BS-ISO-17822 - In vitro diagnostic test systems. Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens. Laboratory quality practice guide
- BS-ISO-18113-2 - Part 2: in Vitro Diagnostic Reagents for Professional Use, Clinidcal Laboratory Testin
- BS-ISO-18113-3 - Part 3: in Vitro Diagnostic Instruments for Professional Use, Clinical Laboratory Test
- BS-ISO-18113-4 - Part 4: in Vitro Diagnostic Reagents for Self-Testing, Clinical Laboratory Testing & I
- BS-ISO-18113-5 - Part 5: in Vitro Diagnostic Instruments for Self-Testing, Clinical Laboratory Testing
- BS-ISO-20658 - Requirements for the collection and transport of samples for medical laboratory examinations
- BS-ISO-35001 - Biorisk management for laboratories and other related organisations
- DD-CEN-ISO-22367 - Medical laboratories. Reduction of error through risk management and continual improvement
- DD-ISO-22367 - Medical Laboratories, Reduction of Error Through Risk Management & Continual Improveme
- PD-ISO-17518 - Medical laboratories. Reagents for staining biological material. Guidance for users
- PD-ISO-17822-1 - In vitro diagnostic test systems. Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens
- PD-ISO-20658 - Medical laboratories. Requirements for collection, transport, receipt, and handling of samples
- PD-ISO-20914 - Medical laboratories. Practical guidance for the estimation of measurement uncertainty
- PD-ISO-22583 - Guidance for supervisors and operators of point-of-care testing (POCT) devices
- PD-ISO-23824 - Medical laboratories. Guidance on application of ISO 15189 in anatomic pathology
- PD-ISO-5441 - Competence requirements for biorisk management advisors
- PD-ISO-5798 - 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
ISO:
- ISO-12771 - Plastics laboratory ware -- Disposable serological pipettes
- ISO-12772 - Laboratory glassware -- Disposable microhaematocrit capillary tubes
- ISO-13130 - Laboratory glassware - Desiccators
- ISO-13132 - Laboratory glassware - Petri dishes
- ISO-15189 - Medical laboratories - Requirements for quality and competence
- ISO-15189 SPANISH - Medical laboratories - Requirements for quality and competence [Standard in Spanish]
- ISO-15190 - Medical laboratories - Requirements for safety
- ISO-15190 SPANISH - Medical laboratories - Requirements for safety [Standard in Spanish]
- ISO-17518 - Medical laboratories - Reagents for staining biological material - Guidance for users
- ISO-17822 - In vitro diagnostic test systems - Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens - Laboratory quality practice guideLaboratory quality practice guide
- ISO-17822-1 - 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
- ISO-20658 - Requirements for the collection and transport of samples for medical laboratory examinations
- ISO-20658 SPANISH - Requirements for the collection and transport of samples for medical laboratory examinations [Standard in Spanish]
- ISO-20914 - Medical laboratories - Practical guidance for the estimation of measurement uncertainty
- ISO-22367 - Medical laboratories - Application of risk management to medical laboratories
- ISO-22367 SPANISH - Medical laboratories - Application of risk management to medical laboratories [Standard in Spanish]
- ISO-22583 - Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipment
- ISO-22869 - Medical laboratories - Guidance on laboratory implementation of ISO 15189: 2003
- ISO-22870 - Point-of-care testing (POCT) - Requirements for quality and competence
- ISO-23162 - Basic semen examination - Specification and test methods
- ISO-23824 - Medical laboratories - Guidance on application of ISO 15189 in anatomic pathology
- ISO-24998 - Plastics laboratory ware - Single-use Petri dishes for microbiological procedures
- ISO-35001 - Biorisk management for laboratories and other related organisations
- ISO-35001-AM1 - - Amendment 1: Biorisk management for laboratories and other related organisations - Amendment 1: Climate action changes
- ISO-35001-AM1 FRENCH - - Amendment 1: Biorisk management for laboratories and other related organisations - Amendment 1: Climate action changes [Standard in French]
- ISO-35001 FRENCH - Biorisk management for laboratories and other related organisations [Standard in French]
- ISO-35001 SPANISH - Biorisk management for laboratories and other related organisations [Standard in Spanish]
- ISO-5798 - 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
- ISO-7713 - Laboratory glassware -- Disposable serological pipettes
Other SDOs:
- EN-ISO-13130 - Laboratory glassware - Desiccators
- EN-ISO-13132 - Laboratory glassware - Petri dishes
- EN-ISO-15189 - Medical laboratories - Requirements for quality and competence
- EN-ISO-22870 - Point-of-care testing (POCT) - Requirements for quality and competence
- SIS-ISO/TS-20658 - Medical laboratories - Requirements for collection, transport, receipt, and handling of samples
- SIS-ISO/TS-22583 - Guidance for supervisors and operators of point-of-care testing (POCT) devices (ISO/TS 22583:2019)
- SS-EN-ISO-13130 - Laboratory glassware - Desiccators (ISO 13130:2011)
- SS-EN-ISO-13132 - Laboratory glassware - Petri dishes (ISO 13132:2011)
- SS-EN-ISO-15189 - Medical laboratories - Requirements for quality and competence (ISO 15189:2022)
- SS-EN-ISO-15195 - Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018)
- SS-EN-ISO-15197 - In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
- SS-EN-ISO-16256 - Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO 16256:2021)
- SS-EN-ISO-19001 - In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
- SS-EN-ISO-21904-4 - Health and safety in welding and allied processes - Equipment for capture and separation of welding fume - Part 4: Determination of the minimum air volume flow rate of capture devices (ISO 21904-4:2020)
- SS-EN-ISO-22367 - Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
- SS-EN-ISO-22870 - Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016)
- SS-EN-ISO-23162 - Basic semen examination - Specification and test methods (ISO 23162:2021)
- SS-EN-ISO-6710 - Single-use containers for human venous blood specimen collection (ISO 6710:2017)
- SS-EN-ISO-6717 - In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)
- SS-ISO-17593 - Clinical laboratory testing and in vitro medical devices Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy (ISO 17593:2022, IDT)
- SS-ISO-20658 - Requirements for the collection and transport of samples for medical laboratory examinations (ISO 20658:2023, IDT)
- SS-ISO-35001 - Biorisk management for laboratories and other related organisations (ISO 35001:2019, IDT)
- UNE-EN-ISO-22870 - Point-of-care testing (POCT) - Requirements for quality and competence