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Clinical Trial Regulations

Clinical Trial Regulations, Total:225 items.

In the international standard classification, Clinical Trial Regulations involves: Medical equipment, Quality, Pharmaceutics, Test conditions and procedures in general, Medical sciences and health care facilities in general, Laboratory medicine, Dentistry, Terminology (principles and coordination), Services, Veterinary medicine, Industrial automation systems, Birth control. Mechanical contraceptives, Applications of information technology, Protection against crime, Protection against fire, Furniture, Woodworking equipment, Waxes, bituminous materials and other petroleum products, Construction materials, Construction equipment, Protective equipment, Products of the textile industry, Home textiles. Linen, Machine tools, Vibrations, shock and vibration measurements, Thermodynamics and temperature measurements.


German Institute for Standardization, Clinical Trial Regulations

  • DIN 6875-3:2008 Special radiotherapy equipments - Part 3: Intensity-modulated radiation therapy - Characteristics, test methods and rules for clinical application
  • DIN 6875-3:2008-03 Special radiotherapy equipments - Part 3: Intensity-modulated radiation therapy - Characteristics, test methods and rules for clinical application
  • DIN EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • DIN EN ISO 8596:2020-05 Ophthalmic optics - Visual acuity testing - Standard and clinical optotypes and their presentation (ISO 8596:2017 + Amd.1:2019); German version EN ISO 8596:2018 + A1:2020
  • DIN EN 14976 Berichtigung 1:2007 Textiles - Mattress ticking - Specifications and test methods; German version EN 14976:2005, Corrigenda to DIN EN 14976:2006-02

Professional Standard - Certification and Accreditation, Clinical Trial Regulations

司法部, Clinical Trial Regulations

RU-GOST R, Clinical Trial Regulations

  • GOST R 52379-2005 Good clinical practice (GCP)
  • 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 51352-1999 Kits of reagents for clinical laboratory diagnostics. Test methods
  • GOST R 51088-1997 Kits of reagents for clinical laboratory diagnostics. General specifications
  • GOST R 54328-2011 Dentistry. Preclinical evaluation of dental implant systems. Animal test methods
  • 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 53079.3-2008 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 53022.2-2008 Clinical laboratory technologies. Requirements for quility of clinical laboratory tests. Part 2. Assessment of methods analytical reliability (accuracy, censitivity, specificity)
  • 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 56701-2015 Medicines for medical applications. Guidance on nonclinical safety studies for the conduct of human clinical trials and marketing authorization for pharmaceuticals
  • GOST ISO 16037-2014 Rubber condoms for clinical trials. Determination of physical properties
  • 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 ISO 230-4-2015 Test code for machine tools. Part 4. Circular tests for numerically controlled machine tools

Group Standards of the People's Republic of China, Clinical Trial Regulations

  • T/CGCPU 014-2020 The practices of chemicals for clinical trials in clinical trial institutions
  • T/CGCPU 024-2023 Specification for training management of practitioners in clinical trial institution
  • T/CGCPU 003-2023 Specification for capacity evaluation of clinical trial institutions
  • T/CGCPU 006-2023 Specification for competency assessment of phase I clinical trials
  • T/CGCPU 024-2022 Specification for training management of practitioners in clinical trial institution
  • T/CGCPU 005-2023 Specification for competency assessment of the clinical trial professional group
  • T/CGCPU 012-2023 Evaluation specifications for archives management of clinical trial institutions
  • T/CGCPU 023-2022 Evaluation standard for clinical trial management system document
  • T/SHDSGY 066-2023 Inspection service specification of clinical trial research center
  • T/CGCPU 023-2023 Evaluation standard for clinical trial management system document
  • T/CGCPU 008-2019 General Auditing Standards for Clinical Trials
  • T/CGCPU 002-2023 Evaluation standard of centralized management of clinical investigational product
  • T/CGCPU 003-2019 Clinical Trial Institution Capacity Evaluation Standards
  • T/CGCPU 006-2019 Phase I Clinical Trial Capacity Evaluation Criteria
  • T/CGCPU 012-2020 File management standards for clinical trial institutions
  • T/CGCPU 022-2022 Evaluation criteria for information management of clinical trials
  • T/CGCPU 022-2023 Evaluation criteria for information management of clinical trials
  • T/CGCPU 005-2019 Clinical Trial Professional Group Competence Evaluation Criteria
  • T/QDAS 108-2023 Technical specification for mobile intelligent clinical examination platform
  • T/CGCPU 015-2020 Requirements for Subjects Risk Monitoring system in clinical trials
  • T/CGCPU 020-2022 Guidelines for the management of pain in clinical trial subjects in the pediatric population
  • T/SAME 003-2021 Norm for establishment of clinical laboratory of measurement integrity
  • T/CGCPU 013-2020 Ethical Considerations for Subject Pain Management in Clinical Trials
  • T/SHQAP 001-2023 Guidelines for the Construction of Quality Management Systems for Drug Clinical Trial Sponsors
  • T/CACM 1351-2021 Standards for collection, preservation and transportation of fecal microbial samples in clinical trials of TCM
  • T/CACM 1353-2021 Technical guidelines for clinical trial design and evaluation of traditional Chinese medicine in the treatment of carotid atherosclerosis
  • T/CGCPU 016-2021 Technical requirements for clinical trials of new drugs for oral inhalation of respiratory system in pediatric populations

Professional Standard - Public Safety Standards, Clinical Trial Regulations

  • GA/T 1970-2021 Standards for forensic clinical examination
  • GA/T 1588-2019 Specifications for the construction of forensic clinical laboratory of forensic science

US-AAMI, Clinical Trial Regulations

Danish Standards Foundation, Clinical Trial Regulations

  • DS/EN ISO 14155:2013 Clinical investigation of medical devices for human subjects - Good clinical practice
  • DS/ISO 16037:2002 Rubber condoms for clinical trials - Measurement of physical properties
  • DS/EN 14976:2005 Textiles - Mattress ticking - Specifications and test methods
  • DS/ISO 230-4:2007 Test code for machine tools - Part 4: Circular tests for numerically controlled machine tools

IT-UNI, Clinical Trial Regulations

Association Francaise de Normalisation, Clinical Trial Regulations

  • NF S99-201*NF EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
  • NF S97-045*NF ISO 16037:2002 Rubber condoms for clinical trials - Measurement of physical properties
  • NF S94-801:2007 Vaginal reinforcement implant for stress urinary incontinence and/or pelvic organ prolapse repair surgery through vaginal approach - Pre-clinical and clinical tests.
  • NF ISO 16037:2002 Préservatifs masculins en caoutchouc destinés aux essais cliniques - Mesurage des propriétés physiques
  • NF P93-400:2013 Temporary edge protection systems - Product specification - Test methods
  • NF G35-108*NF EN 14976:2006 Textiles - Mattress ticking - Specifications and test methods
  • NF E60-096:1998 Test code for machine-tools. Part 4 : circular tests for numerically controlled machine tools.
  • NF E60-100-4*NF ISO 230-4:2022 Test code for machine tools - Part 4 : circular tests for numerically controlled machine tools
  • 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

American Society for Testing and Materials (ASTM), Clinical Trial Regulations

  • ASTM F3108-19 Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Knee Reconstructive Surgery
  • ASTM F3448-20 Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Hip Reconstructive Surgery
  • ASTM E2045-99(2003) Standard Practice for Detailed Clinical Observations of Test Animals
  • ASTM E2045-99(2009) Standard Practice for Detailed Clinical Observations of Test Animals
  • ASTM E2045-99 Standard Practice for Detailed Clinical Observations of Test Animals
  • ASTM E2045-22 Standard Practice for Detailed Clinical Observations of Test Animals
  • ASTM E2045-99(2014) Standard Practice for Detailed Clinical Observations of Test Animals
  • ASTM E1466-92(1999) Standard Specification for Use of Bar Codes on Specimen Tubes in the Clinical Laboratory
  • ASTM F3037-15 Standard Guide for Clinical Trial Design for Hip Replacement Systems (HRSs)
  • ASTM E1246-01 Standard Practice for Reporting Reliability of Clinical Laboratory Computer Systems
  • ASTM E1590-01 Standard Test Method for Fire Testing of Mattresses
  • ASTM E1590-99 Standard Test Method for Fire Testing of Mattresses
  • ASTM E879-01(2007) Standard Specification for Thermistor Sensors for Clinical Laboratory Temperature Measurements
  • ASTM E1590-02 Standard Test Method for Fire Testing of Mattresses
  • ASTM E1590-12 Standard Test Method for Fire Testing of Mattresses
  • ASTM E1590-23 Standard Test Method for Fire Testing of Mattresses
  • ASTM E1590-22 Standard Test Method for Fire Testing of Mattresses
  • ASTM E1590-13 Standard Test Method for Fire Testing of Mattresses
  • ASTM E1590-16 Standard Test Method for Fire Testing of Mattresses
  • ASTM E1590-17 Standard Test Method for Fire Testing of Mattresses
  • 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 E1246-88(1995) Standard Practice for Reporting Reliability of Clinical Laboratory Computer Systems

AT-ON, Clinical Trial Regulations

  • OENORM EN ISO 14155:2021 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)

Lithuanian Standards Office , Clinical Trial Regulations

  • LST EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • LST EN 14976-2005 Textiles - Mattress ticking - Specifications and test methods

PL-PKN, Clinical Trial Regulations

AENOR, Clinical Trial Regulations

  • UNE-EN ISO 14155:2012 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
  • UNE-EN 14976:2006 Textiles - Mattress ticking - Specifications and test methods
  • UNE-ISO 230-4:2008 Test code for machine tools - Part 4: Circular test for numerically controlled machine tools.

British Standards Institution (BSI), Clinical Trial Regulations

  • BS EN ISO 14155:2011 Clinical investigation of medical devices for human subjects. Good clinical practice
  • BS EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Clinical investigation plans
  • BS ISO 230-4:1997 Test code for machine tools - Circular tests for numerically controlled machine tools
  • BS ISO/IEC 10373-7:2008 Identification cards - Test methods - Vicinity cards
  • 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 EN 13398:2003 Methods of test for petroleum and its products - BS 2000-516:Bitumen and bituminous binders - Determination of the elastic recovery of modified bitumen
  • BS EN 13399:2003 Methods of test for petroleum and its products - BS 2000-517:Bitumen and bituminous binders - Determination of storage stability of modified bitumen
  • BS EN 13374:2004 Temporary edge protection systems - Product specification, test methods
  • BS EN 13375:2004 Flexible sheets for waterproofing-Waterproofing of concrete bridge decks and other concrete surfaces trafficable by vehicles-Specimen preparation
  • BS EN 13374:2013 Temporary edge protection systems. Product specification. Test methods
  • BS EN 13374:2013+A1:2018(2021) Temporary edge protection systems. Product specification. Test methods
  • BS EN 14976:2005 Textiles - Mattress tickings - Specification and test methods
  • BS EN 14976:2005(2006) Textiles - Mattress tickings - Specification and test methods
  • BS 4656-1:1981 Accuracy of machine tools and methods of test - Specification for lathes, general purpose type
  • BS EN 13453-2:2004 Bunk beds and high beds for non-domestic use - Test methods
  • BS 4656-13:1983 Accuracy of machine tools and methods of test - Specification for broaching machines, vertical surface type
  • BS 4656-18:1981 Accuracy of machine tools and methods of test - Specification for broaching machines, horizontal internal type
  • BS EN 747-2:2007 Furniture - Bunk beds and high beds for domestic use - Part 2: Test methods
  • BS EN 747-2:2012 Furniture. Bunk beds and high beds. Test methods
  • BS EN 747-2:2008 Furniture. Bunk beds and high beds for domestic use. Test methods
  • BS 4656-37:1989 Accuracy of machine tools and methods of test - Specification for plano-milling machines, gantry type
  • BS EN 1725:1998 Domestic furniture - Beds and mattresses - Safety requirements and test methods

European Committee for Standardization (CEN), Clinical Trial Regulations

  • EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
  • EN 13374:2013 Temporary edge protection systems - Product specification - Test methods
  • EN 14976:2005 Textiles - Mattress ticking - Specifications and test methods

Professional Standard - Medicine, Clinical Trial Regulations

  • YY/T 0991-2015 Clinical trial guideline for orthodontic brackets
  • YY/T 0522-2009 Dentistry Preclinical evaluation of dental implant systems Animal test methods
  • YY/T 1305-2015 Clinical trial guideline for titanium and titanium alloy dental implant
  • YY/T 0990-2015 Clinical trial guideline for polymer-based dental restorative materials

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, Clinical Trial Regulations

卫生健康委员会, Clinical Trial Regulations

Anhui Provincial Standard of the People's Republic of China, Clinical Trial Regulations

Zhejiang Provincial Standard of the People's Republic of China, Clinical Trial Regulations

  • 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

Shanghai Provincial Standard of the People's Republic of China, Clinical Trial Regulations

  • DB31/T 1076-2018 Forensic clinical judicial identification service specification
  • DB31/T 138-10-1994 Transaminase Assay Kit for Clinical Chemistry (Rei's Method)
  • DB31/T 138-9-1994 Total protein assay kit for clinical chemistry (biuret colorimetric method)
  • DB31/T 138-3-1994 Burea Nitrogen Determination Kit for Clinical Chemistry (Diacetyl-Oxime Colorimetric Method)
  • DB31/T 138-4-1994 Urease Nitrogen Determination Kit for Clinical Chemistry (Urease--Berthelot Endpoint Colorimetric Method)
  • DB31/T 138-5-1994 Creatinine Determination Kit for Clinical Chemistry (Picric Acid Endpoint Colorimetric Method)
  • DB31/T 138-8-1994 Total Bilirubin Determination Kit for Clinical Chemistry (Caffeine Colorimetric Method)
  • DB31/T 138-2-1994 Calcium Determination Kit for Clinical Chemistry (Methyl Thymol Blue Colorimetric Method)

Hunan Provincial Standard of the People's Republic of China, Clinical Trial Regulations

  • DB43/T 2135-2021 Technical Service Specifications for the Recruitment and Management of Drug Clinical Trial Subjects

中华人民共和国国家卫生和计划生育委员会, Clinical Trial Regulations

  • WS/T 227-2002 Requirement for the technical procedure manual in clinical laboratory
  • WS/T 228-2002 Preliminary evaluation of quantitative clinical laboratory methods
  • WS/T 124-1999 Inspection criteria of the quality of clinical chemistry in vitro diagnostic kits.General guideline

CU-NC, Clinical Trial Regulations

  • NC 57-50-7-1985 Clinical Methods and Aids Sodium Tungsten Reagent Solution. Quality Specifications
  • NC 57-50-16-1986 Clinical Methods and Aids Mercury Nitrato Reagent Solution. Quality Speeifications
  • NC 57-50-14-1986 Clinical Methods and Aids. Sodium Citrate Reagent Solution. Quality Specifications
  • NC 57-50-15-1986 Clinical Methods and Aids Sodium Carbonate Reagent Solution. Quality Specifications
  • NC 57-50-2-1985 Clinical Methods and Aids. Creatinine, Reference Solution Quality Specifications
  • NC 57-50-1985 Clinical Methods and Aids Solutions. General Quality Specifications
  • NC 57-50-5-1985 Clinical Methods and Aids Sulfurous Acid Solution Quality Specifications
  • NC 57-50-9-1985 Clinical Methods and Aids Reference Solution for Uric Aoid. Quality Specifications
  • NC 57-50-1-1985 Clinical Methods and Aids. Ammonium Molybdate, 2, 5% Solutíon. Quality Specifications
  • NC 20-24-3-1988 Medical Sciences. Auxiliary Ciinical Methods and Means. Lactose Broth Medium. Quality Specifications
  • NC 20-24-2-1988 Medical Sciences. Auxiliary Clinical Methods and Means Thioglicalate Medium. Quality Specifications
  • NC 57-50-11-1985 Clinical Methods and Aids. Phosphotungstic Acid Solution for Uric Acid. Quality Specifications
  • NC 57-50-8-1985 Clinical Methods and Aids Set of Reagents for Determination of Protrombine Time. Quality Specifications
  • NC 57-50-6-1985 Clinical Methods and Aids Saturated Picric Acíd Solution Quality Specifications
  • NC 57-50-17-1986 Clinical Methods and Aids Brominecresol Green Indicator Solution. Quality Specifications
  • NC 57-50-13-1986 Clinical Methods and Aids. Urease Glycerol Reactive Solution. Quality Specifications

International Organization for Standardization (ISO), Clinical Trial Regulations

  • ISO/TS 22911:2016 Dentistry - Preclinical evaluation of dental implant systems - Animal test methods
  • ISO/TS 22911:2005 Dentistry - Preclinical evaluation of dental implant systems - Animal test methods
  • ISO 16037:2002 Rubber condoms for clinical trials - Measurement of physical properties
  • ISO 16037:2002/Amd 1:2011 Rubber condoms for clinical trials — Measurement of physical properties — Amendment 1
  • ISO 230-4:2022 Test code for machine tools — Part 4: Circular tests for numerically controlled machine tools
  • ISO 230-3:2007 Test code for machine tools - Part 3: Determination of thermal effects
  • ISO 230-3:2020 Test code for machine tools - Part 3: Determination of thermal effects

ZA-SANS, Clinical Trial Regulations

  • SANS 16037:2003 Rubber condoms for clinical trials - Measurement of physical properties

未注明发布机构, Clinical Trial Regulations

IX-EU/EC, Clinical Trial Regulations

  • COM(1999) 193 FINAL-1999 Amended Proposal for a European Parliament and Council Directive on the Approximation of the Laws, Regulations and Administrative Provisions of the Member States Relating to the Implementation of Good Clinical Parctice in the Conduct of Clinical Trials on

US-HHS, Clinical Trial Regulations

Korean Agency for Technology and Standards (KATS), Clinical Trial Regulations

  • KS P ISO TS 22911:2010 Dentistry-Preclinical evaluation of dental implant systems-Animal test methods
  • KS P ISO TS 22911:2014 Dentistry-Preclinical evaluation of dental implant systems-Animal test methods
  • KS M ISO 16037:2008 Rubber condoms for clinical trials-Measurement of physical properties
  • KS M ISO 16037:2018 Rubber condoms for clinical trials — Measurement of physical properties
  • 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 4207-2007 Test code for performance and accuracy of numerically controlled lathes
  • KS B 4219-2002 Test conditions for high accuracy turret and single spindle coordinate drilling andboring machines with table of fixed height with vertical spindle-Testing of the accuracy-Part 1:Single column type machines
  • KS B 4207-1981 Test code for performance and accuracy of numerically controlled lathes
  • KS B ISO 230-3:2014 Test code for machine tools — Part 3: Determination of thermal effects
  • KS B ISO 230-3:2009 Test code for machine tools-Part 3:Determination of thermal effects
  • KS B 4918-1995 Machine tools-geometric accuracy tests and practical tests-Test methods
  • KS B 4224-2007 Test code for performance and accuracy of numerically controlled external cylindrical and universal grinding machines
  • KS B 4224-1987 Test code for performance and accuracy of numerically controlled external cylindrical and universal grinding machines

KR-KS, Clinical Trial Regulations

Canadian General Standards Board (CGSB), Clinical Trial Regulations

国家卫生计生委, Clinical Trial Regulations

  • WS/T 503-2017 Blood culture operating procedures in clinical microbiology laboratories
  • WS/T 494-2017 Analysis quality requirements for important routine items in clinical qualitative immunoassay testing

Professional Standard - Agriculture, Clinical Trial Regulations

American Nuclear Society (ANS), Clinical Trial Regulations

Professional Standard - Hygiene , Clinical Trial Regulations

  • WS/T 420-2013 Verification of analytical performance of quantitative kits by clinical laboratory
  • WS/T 406-2012 Analytical quality specifications for routine tests in clinical hematology
  • WS/T 403-2012 Analytical quality specifications for routine analytes in clinical biochemistry

CN-GJB-H, Clinical Trial Regulations

  • GJB 5515/5-2006 Detail specification for clinical laboratory shelter of field mobile medical system

Professional Standard - Forestry, Clinical Trial Regulations

林业部, Clinical Trial Regulations

American National Standards Institute (ANSI), Clinical Trial Regulations

Japanese Industrial Standards Committee (JISC), Clinical Trial Regulations

  • JIS B 6520:1994 Machines planing -- Test and inspection methods
  • JIS T 6001:2005 Preclinical evaluation of biocompatibility of medical devices used in dentistry -- Test methods for dental materials
  • JIS B 6003:1993 Machine tools -- Test methods for vibration
  • JIS B 6202:1986 Test code for performance and accuracy of lathes
  • JIS B 6224:1978 Jig boring machines -- Test conditions for accuracy
  • JIS B 6211:1986 Test code for performance and accuracy of internal cylindrical grinding machines
  • JIS B 6212:1986 Test code for performance and accuracy of external cylindrical and universal grinding machines
  • JIS B 6191:1999 Machine tools -- Geometric accuracy tests and practical tests -- Test methods

CEN - European Committee for Standardization, Clinical Trial Regulations

  • EN 13374:2004 Temporary edge protection systems Product specification@ test methods

Guangdong Provincial Standard of the People's Republic of China, Clinical Trial Regulations

  • DB44/T 2428-2023 Automatic review rules for quantitative biochemical test results in clinical laboratories of traditional Chinese medicine hospitals

Shanxi Provincial Standard of the People's Republic of China, Clinical Trial Regulations

  • DB14/T 2254-2020 Regulations on cold storage and freezing management of clinical in vitro diagnostic reagents in medical institutions

未注明发布机构, Clinical Trial Regulations

IN-BIS, Clinical Trial Regulations

国家市场监督管理总局, Clinical Trial Regulations

  • RB/T 060.2-2021 Forensic Identification/Forensic Science Proficiency Testing Implementation Guide Part 2: Forensic Clinical Identification

国家市场监督管理总局、中国国家标准化管理委员会, Clinical Trial Regulations

  • GB/T 40672-2021 Clinical laboratory testing—Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing

PK-PSQCA, Clinical Trial Regulations

  • PS 882-1972 ACCURACY OF MACHINE TOOLS AND METHODS OF TESTING BROACHING MACHINES HORIZONTAL TYPE




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