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Cytotoxic T cell differentiation process

Cytotoxic T cell differentiation process, Total:166 items.

The international standard classification for "Cytotoxic T cell differentiation process" includes: Other standards related to nuclear energy , Medical Sciences and health care facilities in general , Veterinary medicine , Animal husbandry and breeding , Biology. Botany. Zoology , Pesticides and other agrochemicals , Occupational safety. Industrial hygiene , Laboratory medicine , Transfusion, infusion and injection equipment , Medical equipment in general .

The Chinese standard classification for "Cytotoxic T cell differentiation process" includes: Isotope and radioactive sources in general , Marking, packaing, transport and storage , Animal quarantine, veterinary and epidemic prevention , Domesticate animal , Basic Subject in general , Basic standards and general methods , Pesticide management and application method , Medical apparatus and devices in general , Labor sanitation , Medical laboratory equipment , General and microsurgical devices , Sanitation in general .


Group Standards of the People's Republic of China

  • T/CGCPU 009-2020 Control requirements for the preparation process of immune cell products
  • T/CECCEDA 003.1-2023 Technical requirement of single-use materials in CAR-T production Part 1: Cell frozen bag、Cell storage bag
  • T/CI 059-2022 Circulating epithelial cell separator
  • T/SHSYCXH 8-2022 Test method of human Natural Killer cells and Natural Killer T cells from peripheral blood-Flow cytometry
  • T/CECCEDA 002-2023 Manufacture practice of single-use materials in CAR-T production
  • T/CIRA 1-2020 Radiation grafted filtration membranes for leukocyte reduction
  • T/CGCPU 017-2021 Quality control requirements for clinical research of CAR-T cell products
  • T/CECCEDA 003.2-2023 Technical requirement of single-use materials in CAR-T production Part 2: Cell sap culture tank
  • T/SDHCST 007-2023 Procedures for Repeated Dose Toxicity Testing of the Cell Therapy Medical Products
  • T/CECCEDA 003.4-2023 Technical requirement of single-use materials in CAR-T production Part 4: Connect joint
  • T/ZPP 017-2023 Mass Cytometry Analyzer
  • T/SHPPA 011-2021 Autologous CAR-T cell therapy medication supply chain management specifications
  • T/CAMDI 023-2019 Polyester filtration membrane for Leukocyte reduction filters
  • T/GDC 213-2023 Cell Strainers
  • T/SDHCST 001-2022 Technical Specification for Artificially Induced Pluripotent Stem Cells to Differentiate into Neural Cells
  • T/SDHCST 006-2023 Procedures for Single Dose Toxicity Testing of the Cell Therapy Medical Products
  • T/SDHCST 008-2023 Procedures for Immunogenicity and Immunotoxicity of the Cell Therapy Medical Products

Professional Standard - Pharmaceutical Packaging

Professional Standard - Agriculture

  • 259药典 三部-2010 Appendix Ⅹ XR Anti-human T cell immunoglobulin titer assay (lymphocytotoxicity test)
  • 279药典 四部-2015 3500 Biological activity-potency assay 3516 Anti-human T cell immunoglobulin potency assay (lymphocytotoxicity test)
  • 327药典 三部-2020 Biological activity-potency assay 3516 Anti-human T cell immunoglobulin potency assay (lymphocytotoxicity test)
  • 315药典 四部-2020 4000 Testing method for pharmaceutical packaging materials 4014 Cytotoxicity testing method for pharmaceutical packaging materials
  • 274药典 四部-2020 3500 Biological activity-potency assay 3516 Anti-human T cell immunoglobulin potency assay (lymphocytotoxicity test)
  • 298药典 三部-2015 Biological activity-potency assay 3516 Anti-human T cell immunoglobulin potency assay (lymphocytotoxicity test) General 129

Professional Standard - Commodity Inspection

  • SN/T 2242-2008 Natural killer cell activity assay
  • SN/T 3824-2014 Phototoxicity test for cosmetics - Determination of recombinant red blood cell
  • SN/T 1919-2007 Protocol of hemagglutination inhibition test for porcine parvovirus
  • SN/T 2328-2009 Cosmetics acute toxicity of keratinocyte cytotoxicity test
  • SN/T 2330-2009 Cosmetics embryotoxicity and developmental toxicity of mice embryonic stem cell test

中华人民共和国国家质量监督检验检疫总局、中国国家标准化管理委员会

Professional Standard - Aquaculture

Jilin Provincial Standard of the People's Republic of China

  • DB22/T 2853-2017 Peripheral Blood High Fluorescence Intensity Lymphocyte Percentage (HFLC%) Screening Technical Regulations for Atypical Lymphocytes
  • DB22/T 2565-2016 Influenza virus MDCK cell virus isolation and detection method

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

  • GB/T 38506-2020 Determination of biochemical parameters in animal cell culture process
  • GB/T 41895-2022 Determination for DNA viruses of cell—MNP marker method
  • GB/T 38506-2020(英文版) Determination of biochemical parameters in animal cell culture process
  • GB/T 42076.1-2022 Biotechnology—Cell counting—Part 1: General guidance on cell counting methods
  • GB/T 15670.17-2017 Toxicological test methods for pesticides registration. Part 17: Mammalian spermatogonial/spermatocyte chromosome aberration test
  • GB/T 41915-2022 Nanotechnologies―In vitro MTS assay for measuring the cytotoxic effect of nanoparticles
  • GB/T 16886.5-2003 Biological evaluation of medical devices - Part 5: Test for in vitro cytotoxicity
  • GB/T 14926.63-2001 Laboratory animal-Method for examination of Simian T Lymphotropic Virus type 1 (STLV-1)

农业农村部

National Metrological Verification Regulations of the People's Republic of China

  • JJG 714-1990 Verification Regulation of Blood Cell Analyzer
  • JJG 714-2012 Verification Regulation of Blood Cell Analyzers

未注明发布机构

  • DIN EN 16418 E:2012-04 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)

Occupational Health Standard of the People's Republic of China

  • GBZ/T 240.13-2011 Evaluation procedure and test methods for chemical toxicology - Part 13: Chromosomal aberration test for mammalian spermatogonium/primary spermatocyte
  • GBZ/T(卫生) 240.13-2011 Procedures and tests for toxicological evaluations of chemicals—Part 13:Mammalian spermatogonium/primary spermatocyte chromosome aberration test

Anhui Provincial Standard of the People's Republic of China

  • DB34/T 3987-2021 Technical regulations for cell culture isolation and detection of avian leukosis virus

Taiwan Provincial Standard of the People's Republic of China

  • CNS 14393-5-2004 Biological evaluation of medical devices – Part 5:Tests for in vitro cytotoxicity

Professional Standard - Medicine

  • YY 0329-2009 Leukocyte reduction filters for single use
  • YY/T 1236-2014 Cytomegalovirus(CMV)IgG/IgM antibody detection kit
  • YY/T 0870.3-2013 Test for genotoxicity of medical devices - Part 3: In vitro mammalian cell gene mutation test using mouse lymphoma cell
  • YY 0329-2002 Leukocyte removal filters for single use

海关总署

  • SN/T 5159-2019 Chemicals-Transgenic rodent somatic and germ cell gene mutation assays

Professional Standard - Hygiene

American Society for Testing and Materials (ASTM)

  • ASTM F3354-19 Standard Guide for Evaluating Extracellular Matrix Decellularization Processes
  • ASTM E2526-22 Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
  • ASTM F895-11(2016) Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
  • ASTM F895-84(2001) Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
  • ASTM E2526-08 Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
  • ASTM F895-84(2006) Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
  • ASTM F895-84(2001)e1 Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
  • ASTM E2526-08(2013) Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
  • ASTM D3576-20 Standard Test Method for Cell Size of Rigid Cellular Plastics
  • ASTM E1482-12(2017) Standard Practice for Use of Gel Filtration Columns for Cytotoxicity Reduction and Neutralization
  • ASTM E1482-12 Standard Practice for Use of Gel Filtration Columns for Cytotoxicity Reduction and Neutralization
  • ASTM E1482-23 Standard Practice for Use of Gel Filtration Columns for Cytotoxicity Reduction and Neutralization
  • ASTM D6226-21 Standard Test Method for Open Cell Content of Rigid Cellular Plastics
  • ASTM F3368-19 Standard Guide for Cell Potency Assays for Cell Therapy and Tissue Engineered Products
  • ASTM F3206-17 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies
  • ASTM E1398-91(2003) Standard Practice for the in vivo Rat Hepatocyte DNA Repair Assay

SCC

  • AS 2567:1982 Cytotoxic drug safety cabinets
  • AS 2567:1994 Laminar flow cytotoxic drug safety cabinets
  • AWWA ACE68896 Comparative Cytotoxicity and Genotoxicity of Priority DBPs
  • AAMI BF64:2012 Leukocyte reduction filters
  • AAMI BF64:2002(R2011) Leukocyte reduction filters
  • AWWA WQTC52850 Infectious Cryptosporidium parvum Detection by Cell Culture and PCR or Cell Culture and Antibodies?
  • AS 2639:1983 Cytotoxic drug safety cabinets - Installation and use
  • NS-EN 16418:2014 Paper and board — Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • DANSK DS/EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • NS-EN 15845:2010 Paper and board — Determination of the cytotoxicity of aqueous extracts
  • DANSK DS/EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
  • AWWA WQTC65810 Host Cell Capture Quantitative PCR Detection of Viruses
  • DIN EN 16418 E:2012 Draft Document - Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2); German version prEN 16418:2012
  • AWWA WQTC56996 Monitoring Honolulu's Groundwater Sources for Human Enteric Viruses Using Cell Culture and Cell-Culture PCR
  • AWWA WQTC50408 Identification of Viruses Present in Ground Water Cell Culture Harvest by PCR
  • DANSK DS/ISO 20391-1:2018 Biotechnology – Cell counting – Part 1: General guidance on cell counting methods
  • 12/30259424 DC BS EN 16418. Paper and board. Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • DANSK DS/ISO 21115:2019 Water quality – Determination of acute toxicity of water samples and chemicals to a fish gill cell line (RTgill-W1)
  • DIN EN 15845 E:2008 Draft Document - Paper and board - Determination of the cytotoxicity of aqueous extracts; German version prEN 15845:2008
  • AWWA ACE63225 Mammalian Cell Toxicity of Emerging Drinking Water Disinfection Byproducts
  • BS PD CEN/TS 17688-1:2021 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for Fine Needle Aspirates (FNAs)-Isolated cellular RNA
  • 08/30183128 DC BS EN 15845. Paper and board. Determination of the cytotoxicity of aqueous extracts
  • BS 1335:1946 Specification for air depolarized primary cells
  • AWWA WQTC56953 Detection of Infectious Adenovirus by mRNA RT-PCR in Cell Culture
  • AAMI/ISO 10993-5:1999 Biological evaluation of medical devices - Part 5: Tests for In Vitro Cytotoxicity

KR-KS

  • KS M ISO 4590-2018 Rigid cellular plastics — Determination of the volume percentage of open cells and of closed cells
  • KS P ISO 10993-5-2018(2023) Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity
  • KS J ISO 20391-1-2019 Biotechnology — Cell counting — Part 1: General guidance on cell counting methods

Korean Agency for Technology and Standards (KATS)

  • KS M ISO 4590:2018 Rigid cellular plastics — Determination of the volume percentage of open cells and of closed cells
  • KS P ISO 10993-5-2023 Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity
  • KS J ISO 20391-1:2019 Biotechnology — Cell counting — Part 1: General guidance on cell counting methods

Association Francaise de Normalisation

  • NF EN 16418:2014 Paper and cardboard - Determination of the cytotoxic effect of aqueous extracts using a hepatoma cell line possessing metabolic enzymes (HepG2 cells)
  • NF S91-142:1988 Dental implants. Cytocompatibility. Study of cellular proliferation.
  • NF S91-145:1988 Dentistry. Dental implants. Cytocompatibility. Study of cells attachment and spreading on the biomaterial.
  • NF Q03-111*NF EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • NF S91-143:1988 Dental implants. Cytocompatibility. Study of total cellular proteins.
  • NF S91-144:1988 Dental implants. Cytocompatibility. Evaluation of 51CR extracellular release.
  • NF Q03-098*NF EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
  • NF EN 15845:2010 Paper and cardboard - Determination of the cytotoxicity of aqueous extracts
  • NF S91-146:1988 Dental implants. Cytocompatibility. Study of cellular multiplication, migration and adherence.
  • NF ISO 21115:2019 Water quality - Determination of acute toxicity of water samples and chemicals to fish gill cell line (RTgill-W1)
  • NF T90-723*NF ISO 21115:2019 Water quality - Determination of acute toxicity of water samples and chemicals to a fish gill cell line (RTgill-W1)

Standard Association of Australia (SAA)

  • AS 2567:2002 Laminar flow cytotoxic drug safety cabinets
  • AS 2639:1994 Laminar flow cytotoxic drug safety cabinets - Installation and use

American National Standards Institute (ANSI)

US-AAMI

API - American Petroleum Institute

European Committee for Standardization (CEN)

  • EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
  • EN ISO 20186-3:2019 Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019)

British Standards Institution (BSI)

  • BS EN 16418:2014 Paper and board. Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • 23/30466937 DC BS ISO 24479 Biotechnology — Cellular morphological analysis — General requirements and considerations for cell morphometry to quantify cell morphological features
  • BS EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
  • BS ISO 21115:2019 Water quality. Determination of acute toxicity of water samples and chemicals to a fish gill cell line (RTgill-W1)
  • PD CEN/TS 17688-1:2021 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for Fine Needle Aspirates (FNAs). Isolated cellular RNA
  • BS EN ISO 10993-5:1999 Biological evaluation of medical devices - Tests for in vitro cytotoxicity

AENOR

  • UNE-EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • UNE-EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts

International Organization for Standardization (ISO)

  • ISO/DIS 24479:2023 Biotechnology — Cellular morphological analysis — General requirements and considerations for cell morphometry to quantify cell morphological features
  • ISO 20186-3:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma
  • ISO 20391-1:2018 Biotechnology - Cell counting - Part 1: General guidance on cell counting methods
  • ISO 21115:2019 Water quality — Determination of acute toxicity of water samples and chemicals to a fish gill cell line (RTgill-W1)

Lithuanian Standards Office

  • LST EN 15845-2010 Paper and board - Determination of the cytotoxicity of aqueous extracts

German Institute for Standardization

  • DIN EN 16418:2014-07 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2); German version EN 16418:2014
  • DIN EN 15845:2010-05 Paper and board - Determination of the cytotoxicity of aqueous extracts; German version EN 15845:2010
  • DIN 58932-2:1998-06 Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
  • DIN 58932-2:1998 Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
  • DIN 12980:2005 Laboratory furniture - Safety cabinets for handling cytotoxic substances
  • DIN 58932-4:2003 Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes
  • DIN EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2); German version EN 16418:2014

Danish Standards Foundation

  • DS/EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts

GSO

  • GSO ASTM F3206:2022 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies
  • BH GSO ASTM F3206:2023 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies
  • BH GSO ISO 10993-5:2017 Biological evaluation of medical devices -- Part 5: Tests for in vitro cytotoxicity

GOST

IT-UNI

  • UNI ISO 20391-1:2021 Biotechnology - Cell counting - Part 1: General guidance on cell counting methods

RU-GOST R

  • GOST R 54496-2011 Water. The determination of toxicity with use of green freshwater unicellular algae

Military Standards (MIL-STD)

CZ-CSN

  • CSN 57 0539-1999 Automatedestimation of the bacteria count in raw milk by direct count the bacterial cells

VN-TCVN

  • TCVN 7391-5-2005 Biological evaluation of medical devices.Part 5: Tests for in vitro cytotoxicity