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clinical laboratory staff
clinical laboratory staff, Total:140 items.
In the international standard classification, clinical laboratory staff involves: Medical sciences and health care facilities in general, ENVIRONMENT. HEALTH PROTECTION. SAFETY, Laboratory medicine, Hospital equipment, Sensory analysis, Medical equipment, Applications of information technology, Construction materials, Pharmaceutics, Test conditions and procedures in general, Thermodynamics and temperature measurements, Welding, brazing and soldering, Vibration and shock with respect to human beings, Earth-moving machinery, Construction equipment, Radiation protection, Nuclear energy engineering, Quality, Company organization and management, Agricultural machines, implements and equipment, Environmental protection, Vibrations, shock and vibration measurements, Protective equipment, Industrial trucks, Protection against dangerous goods.
RU-GOST R, clinical laboratory staff
- GOST R 53079.3-2008 Medical laboratory technologies. Quality assurance of clinical laboratory tests. Part 3. Rules for interaction between personnel of clinical departments and personnel of clinical-diagnostic laboratory in medical institutions during fulfillment of clinical
- GOST R 53022.3-2008 Clinical laboratory technologies. Requirements of quality of clinical laboratory tests. Part 3. Assessment of laboratory tests clinical significance
- GOST R 53022.4-2008 Medical laboratory technologies. Requirement of quality of clinical laboratory tests. Part 4. Rules for development of requirements to timeliness of laboratory information submitting
- GOST R 53079.2-2008 Medical laboratory technologies. Quality assurance of clinical laboratory tests. Part 2. Guidelines for improvements of quality in clinical-diagnostic laboratory. Typical model
- GOST R 53022.2-2008 Clinical laboratory technologies. Requirements for quility of clinical laboratory tests. Part 2. Assessment of methods analytical reliability (accuracy, censitivity, specificity)
- GOST R 53133.1-2008 Clinical laboratory technologies. Quality control of clinical laboratory tests. Part 1. Limits of allowable errors of the results of the analyte measurements in clinical-diagnostics laboratories
- GOST R 56701-2015 Medicines for medical applications. Guidance on nonclinical safety studies for the conduct of human clinical trials and marketing authorization for pharmaceuticals
- GOST R 53133.3-2008 Medical laboratory technologies. Quality control of clinical laboratory tests. Description of materials for quality control of clinical laboratory investigations
- GOST R 53133.4-2008 Medical laboratory technologies. Quality control of clinical laboratory tests. Part 4. Rules for conducting of clinical audit of efficiency of laboratory provision of medical institution activity
- GOST ISO 13300-1-2015 Sensory analysis. General guidance for the staff of a sensory evaluation laboratory. Part 1. Staff responsibilities
- GOST ISO 17593-2011 Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
Professional Standard - Hygiene , clinical laboratory staff
- WS/T 251-2005 Guidelines for Clinical Laboratory Safety
- WS/T 442-2014 Guideline for clinical laboratory biosafety
- WS/T 249-2005 Clinical Laboratory Waste Management
- WS/T 418-2013 Guidelines for the selection of referral clinical laboratories
- WS/T 250-2005 Requirements of Quality Assurance for Clinical Laboratories
- WS/T 255-2005 Clinical laboratory medicine Reguirements for reference measurement laboratories
- WS/T 489-2016 Clinical microbiological laboratory diagnosis of urinary tract infection;
- WS/T 489-2015 Clinical Microbiological Laboratory Diagnosis of Urinary Tract Infection
- WS/T 402-2012 Define and determine the reference intervals in clinical laboratory
- WS/T 420-2013 Verification of analytical performance of quantitative kits by clinical laboratory
General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, clinical laboratory staff
- GB/T 20469-2006 General guideline of the clinical laboratory design
- GB/T 20470-2006 Requirements of external quality assessment for clinical laboratories
- GB/T 20468-2006 Guideline for internal quality control for quantitative measurements in clinical laboratory
- GB/T 23470.1-2009 Sensory analysis.General guidance for the staff of a sensory evaluation laboratory.Part 1:Staff reponsibilities
中华人民共和国国家卫生和计划生育委员会, clinical laboratory staff
- WS/T 496-2017 Quality indicators in clinical laboratories
- WS/T 498-2017 Performance guideline for clinical laboratory diagnosis of bacterial diarrhea
- WS/T 497-2017 Performance guideline for clinical laboratory diagnosis of invasive fungal diseases
US-HHS, clinical laboratory staff
Group Standards of the People's Republic of China, clinical laboratory staff
- T/CGCPU 024-2023 Specification for training management of practitioners in clinical trial institution
- T/CGCPU 024-2022 Specification for training management of practitioners in clinical trial institution
- T/SAME 003-2021 Norm for establishment of clinical laboratory of measurement integrity
- T/SAME 001-2022 Management requirements for level II biosafety cabinets in clinical laboratories
- T/CAS 651-2022 Guidelines for hiring, competency development and assessment supervision of Inspection and testinglaboratory personnel
- T/AHEMA 7-2021 Classification and accreditation for staff of laboratory analysis of ecological environmental monitoring body
ASHRAE - American Society of Heating@ Refrigerating and Air-Conditioning Engineers@ Inc., clinical laboratory staff
AENOR, clinical laboratory staff
- UNE 129001:1997 CLINICAL LABORATORY REPORTS. PREPARING REQUIREMENTS.
- UNE 129002:2000 IN Glossary of recommended terms in clinical laboratory sciences.
- UNE-EN ISO 18812:2003 Health informatics - Clinical analyser interfaces to laboratry information systems - Use profiles (ISO 18812:2003)
卫生健康委员会, clinical laboratory staff
- WS/T 574-2018 Purified water for clinical laboratory reagents
- WS/T 616-2018 Automated review of quantitative test results in clinical laboratories
Zhejiang Provincial Standard of the People's Republic of China, clinical laboratory staff
- DB33/T 903-2013 Classification and coding of clinical laboratory test items
- DB33/T 893.3-2013 Clinical Laboratory Information System Part 3: Workflow Specification
- DB33/T 893.1-2013 Clinical Laboratory Information System Part 1: Basic Functional Specifications
- DB33/T 893.2-2013 Clinical Laboratory Information System Part 2: Data Transmission and Exchange
US-CLSI, clinical laboratory staff
- CLSI GP17-A3-2012 Clinical Laboratory Safety; Approved Guideline - Third Edition
- CLSI C28-A3c-2008 Defining, Establishing, and Verifying Reference Intervals in the Clinical laboratory
- CLSI MM19-A-2011 Establishing Molecular Testing in Clinical Laboratory Environments; Approved Guideline
- CLSI C56-A-2012 Hemolysis, Icterus, and Lipemia/Turbidity Indices as Indicators of Interference in Clinical Laboratory Analysis; Approved Guideline
US-FCR, clinical laboratory staff
国家卫生计生委, clinical laboratory staff
- WS/T 503-2017 Blood culture operating procedures in clinical microbiology laboratories
Korean Agency for Technology and Standards (KATS), clinical laboratory staff
- KS P 8428-2015(2020) General requirements for clinical laboratory automation system performance
- KS P 8429-2015(2020) General requirements for clinical laboratory automation system information
- KS P 8430-2015(2020) Management and safety requirements for clinical laboratory pre-analytical automation system
- KS X ISO 18812-2016(2021) Health informatics — Clinical analyser interfaces to laboratory information systems — Use profiles
- KS P ISO TR 18112:2009 Clinical laboratory testing and in vitro diagnostic test systems-In vitro diagnostic medical devices for professional use-Summary of regulatory requirements for information supplied by the manufacturer
- KS Q ISO 13300-1-2007(2012) Sensory analysis－General guidance for the staff of a sensory evaluation laboratory－Part 1：Staff responsibilities
- KS Q ISO 13300-1-2007(2021) Sensory analysis－General guidance for the staff of a sensory evaluation laboratory－Part 1：Staff responsibilities
- KS P ISO 15198:2006 Clinical laboratory medicine-In vitro diagnostic medical devices-Validation of user quality control procedures by the manufacturer
- KS P ISO 15198:2017 Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer
- KS P ISO TS 16782:2018 Clinical laboratory testing ─ Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing
- KS P ISO 17593-2009(2019) Clinical laboratory testing and in vitro medical devices－Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
- KS P ISO 17593:2009 Clinical laboratory testing and in vitro medical devices－Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
- KS P ISO TR 18112-2009(2014) Clinical laboratory testing and in vitro diagnostic test systems－In vitro diagnostic medical devices for professional use－Summary of regulatory requirements for information supplied by the manufacture
- KS B ISO 18436-5:2018 Condition monitoring and diagnostics of machines — Requirements for qualification and assessment of personnel — Part 5:Lubricant laboratory technician/analyst
American Society for Testing and Materials (ASTM), clinical laboratory staff
- ASTM E1466-92(1999) Standard Specification for Use of Bar Codes on Specimen Tubes in the Clinical Laboratory
- ASTM E792-95e1 Standard Guide for Selection of a Clinical Laboratory Information Management System
- ASTM E792-02 Standard Guide for Selection of a Clinical Laboratory Information Management System
- ASTM E1246-88(1995) Standard Practice for Reporting Reliability of Clinical Laboratory Computer Systems
- ASTM E1029-84(1997) Standard Guide for Documentation of Clinical Laboratory Computer Systems
- ASTM E1639-97 Standard Guide for Functional Requirements of Clinical Laboratory Information Management Systems
- ASTM E1029-01 Standard Guide for Documentation of Clinical Laboratory Computer Systems
- ASTM E102-93(1997) Standard Test Method for Saybolt Furol Viscosity of Bituminous Materials at High Temperatures
- ASTM E1639-01 Standard Guide for Functional Requirements of Clinical Laboratory Information Management Systems
- ASTM E1246-01 Standard Practice for Reporting Reliability of Clinical Laboratory Computer Systems
- ASTM E879-01(2007) Standard Specification for Thermistor Sensors for Clinical Laboratory Temperature Measurements
- ASTM E879-01 Standard Specification for Thermistor Sensors for Clinical Laboratory Temperature Measurements
- ASTM E879-93 Standard Specification for Thermistor Sensors for Clinical Laboratory Temperature Measurements
- ASTM E1381-95 Standard Specification for Low-Level Protocol to Transfer Messages Between Clinical Laboratory Instruments and Computer Systems
- ASTM E1381-02 Standard Specification for Low-Level Protocol to Transfer Messages Between Clinical Laboratory Instruments and Computer Systems
Heilongjiang Provincial Standard of the People's Republic of China, clinical laboratory staff
- DB23/T 3598-2023 Hemp Inspection and Testing Laboratory Personnel Competency Requirements
Professional Standard - Commodity Inspection, clinical laboratory staff
- SN/T 2752.4-2011 Self-protection specifications for health and quarantine personnel Part 4: Laboratory personnel
British Standards Institution (BSI), clinical laboratory staff
- DD ENV 13728-2001 Health informatics. Clinical analyser interfaces to laboratory information systems
- BS EN ISO 7096:2009 Earth-moving machinery. Laboratory evaluation of operator seat vibration
- BS EN ISO 7096:2008 Earth-moving machinery - Laboratory evaluation of operator seat vibration
- BS PD ISO/TS 16782:2016 Clinical laboratory testing. Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing
- BS ISO 8084:2003 Machinery for forestry - Operator protective structures - Laboratory tests and performance requirements
- BS ISO 13300-2:2006 Sensory analysis - General guidance for the staff of a sensory evaluation laboratory - Recruitment and training of panel leaders
- BS ISO 15198:2004 Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer
- BS ISO 18436-5:2012 Condition monitoring and diagnostics of machines. Requirements for qualification and assessment of personnel. Lubricant laboratory technician/analyst
- BS ISO 17593:2022 Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
- BS ISO 17593:2007 Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
- 21/30402425 DC BS ISO 17593. Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for selftesting of oral anticoagulant therapy
Guangdong Provincial Standard of the People's Republic of China, clinical laboratory staff
- DB44/T 2428-2023 Automatic review rules for quantitative biochemical test results in clinical laboratories of traditional Chinese medicine hospitals
Association Francaise de Normalisation, clinical laboratory staff
- NF EN ISO 18812:2003 Informatique de santé - Interfaces d'analyseur clinique pour systèmes d'information de laboratoire - Profils d'utilisation
- NF ISO 13300-1:2006 Analyse sensorielle - Guide général à l'attention du personnel des laboratoires d'analyse sensorielle - Partie 1 : responsabilités du personnel
- NF E90-411/IN1*NF EN 13490/IN1:2009 Mechanical vibration - Industrial trucks - Laboratory evaluation and specification of operator seat vibration.
- NF E90-411*NF EN 13490+A1:2009 Mechanical vibration - Industrial trucks - Laboratory evaluation and specification of operator seat vibration
- NF S92-012*NF EN ISO 16256:2013 Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases
German Institute for Standardization, clinical laboratory staff
- DIN 58937-7:1994 General laboratory medicine (clinical pathology); part 7: listing of features of in vitro diagnostic systems
- DIN 25425-4 Beiblatt 2:2023-01 Radionuclide Laboratories - Part 4: Rules for the protection of persons; Supplement 2: Guidance notes on shielding of gamma- and beta-radiation / Note: Date of issue 2022-11-25*Intended as replacement for DIN 25425-4 Beiblatt 2 (2013-02).
- DIN 25425-4:2012 Radioisotope laboratories - Part 4: Rules for the protection of persons
- DIN 25425-4:2019-12 Radioisotope laboratories - Part 4: Rules for the protection of persons
- DIN 25425-4 Beiblatt 2:2013-02 Radioisotope laboratories - Part 4: Rules for the protection of persons; Guidance notes on shielding of gamma- and beta-radiation / Note: To be replaced by DIN 25425-4 Beiblatt 2 (2023-01).
- DIN EN ISO 18812:2003 Health informatics - Clinical analyser interfaces to laboratory information systems - Use of profiles (ISO 18812:2003); German version EN ISO 18812:2003, text in English
- DIN EN ISO 18812:2003-07 Health informatics - Clinical analyser interfaces to laboratory information systems - Use of profiles (ISO 18812:2003); German version EN ISO 18812:2003, text in English
Professional Standard - Public Safety Standards, clinical laboratory staff
- GA/T 1147-2014 Labortory specifications for examination of ethanol concentration in driver's blood
Association of German Mechanical Engineers, clinical laboratory staff
Japanese Industrial Standards Committee (JISC), clinical laboratory staff
- JIS A 8304:2001 Earth-moving machinery -- Laboratory evaluation of operator seat vibration
- JIS A 8922:2001 Earth-moving machinery -- Hydraulic excavators -- Laboratory tests and performance requirements for operator protective guards
国家市场监督管理总局、中国国家标准化管理委员会, clinical laboratory staff
- GB/T 40672-2021 Clinical laboratory testing—Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing
- GB/T 22576.4-2021 Medical laboratories—Requirements for quality and competence—Part 4: Requirements in the field of clinical chemistry examination
- GB/T 22576.2-2021 Medical laboratories—Requirements for quality and competence—Part 2: Requirements in the field of clinical hematological examination
- GB/T 22576.5-2021 Medical laboratories—Requirements for quality and competence—Part 5: Requirements in the field of clinical immunology examination
- GB/T 22576.6-2021 Medical laboratories—Requirements for quality and competence—Part 6: Requirements in the field of clinical microbiological examination
International Organization for Standardization (ISO), clinical laboratory staff
- ISO/TR 18112:2006 Clinical laboratory testing and in vitro diagnostic test systems - In vitro diagnostic medical devices for professional use - Summary of regulatory requirements for information supplied by the manufacturer
- ISO 15198:2004 Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer
- ISO 8084:1993 Machinery for forestry; operator protective structures; laboratory tests and performance requirements
- ISO 17593:2022 Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
- ISO 11613:2017 Protective clothing for firefighter's who are engaged in support activities associated with structural fire fighting — Laboratory test methods and performance
- ISO 18436-5:2012 Condition monitoring and diagnostics of machines - Requirements for qualification and assessment of personnel - Part 5: Lubricant laboratory technician/analyst
- ISO 17593:2007 Clinical laboratory testing and in vitro medical devices - Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
KR-KS, clinical laboratory staff
- KS P ISO 15198-2017 Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer
- KS P ISO TS 16782-2018 Clinical laboratory testing ─ Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing
- KS X ISO 18812-2016 Health informatics — Clinical analyser interfaces to laboratory information systems — Use profiles
- KS P ISO 15198-2017(2022) Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer
- KS B ISO 18436-5-2018 Condition monitoring and diagnostics of machines — Requirements for qualification and assessment of personnel — Part 5:Lubricant laboratory technician/analyst
American National Standards Institute （ANSI), clinical laboratory staff
- ANSI/HL7 V3 PORT, R 1-2004 HL7 Version 3 Standard: Regulated Studies - Periodic Reporting of Clinical Trials Laboratory Results, , Release 1
European Committee for Standardization (CEN), clinical laboratory staff
- DD ENV 13728-2000 Health Informatics - Clinical Analyser Interfaces to Laboratory Information Systems Ratified European Text
- EN ISO 7096:2008 Earth-moving machinery - Laboratory evaluation of operator seat vibration (ISO 7096:2000)
Danish Standards Foundation, clinical laboratory staff
- DS/EN ISO 18812:2003 Health informatics - Clinical analyser interfaces to laboratry information systems - Use profiles (ISO 18812:2003)
- DS/ISO 18436-5:2013 Condition monitoring and diagnostics of machines - Requirements for qualification and assessment of personnel - Part 5: Lubricant laboratory technician/analyst
Lithuanian Standards Office , clinical laboratory staff
- LST EN ISO 18812:2003 Health informatics - Clinical analyser interfaces to laboratry information systems - Use profiles (ISO 18812:2003)
Indonesia Standards, clinical laboratory staff
- SNI ISO 15198:2009 Clinical laboratory medicine - In vitro diagnostic medical devices - validation of user quality control procedures by the manufacturer
US-CFR-file, clinical laboratory staff
- CFR 42-405.209-2013 Public Health. Part405:Federal health insurance for the aged and disabled. Section405.209:Payment for a non-experimental/investigational (Category B)device.
- CFR 42-405.203-2013 Public Health. Part405:Federal health insurance for the aged and disabled. Section405.203:FDA categorization of investigational devices.
Professional Standard - Medicine, clinical laboratory staff
- YY/T 0690-2008 Clinical laboratory testing and in vitro medical devices -- Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy