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Cell passage stability

Cell passage stability, Total:128 items.

The international standard classification for "Cell passage stability" includes: Biology. Botany. Zoology , Plant growing , Medical Sciences and health care facilities in general , Laboratory medicine , Transfusion, infusion and injection equipment , Medical equipment in general , Lubricants, industrial oils and related products .

The Chinese standard classification for "Cell passage stability" includes: Basic Subject in general , Agriculture and forestry technology , Biological agent and blood products , Marking, packaing, transport and storage , Sanitation in general , Medical laboratory equipment , General and microsurgical devices , Medical apparatus and devices in general .


Group Standards of the People's Republic of China

  • T/CIET 503-2024 Specification for preparation and quality identification of hepatic progenitor cells derived from human induced pluripotent stem cells
  • T/CEAC 039-2024 Stem cell identification methods
  • T/CECCEDA 003.2-2023 Technical requirement of single-use materials in CAR-T production Part 2: Cell sap culture tank
  • T/LTIA 17-2022 Guidelines for the detection of genomic instability in human cells
  • T/CECCEDA 003.1-2023 Technical requirement of single-use materials in CAR-T production Part 1: Cell frozen bag、Cell storage bag
  • T/CSTE 0379-2023 Identification and Cytoactivity Determination of Bioactive Peptides
  • T/CSCB 0008-2021 Primary human hepatocyte
  • T/WEBIO 0001-2023 Specification of human primary cell preparation and quality control
  • T/ZZB 1653-2020 Disposable cell cryogenic vials(Polypropylene)

Professional Standard - Agriculture

  • 289药典 四部-2015 3500 Biological Activity-Potency Assay 3526 Recombinant Human Granulocyte Macrophage Stimulating Factor Biological Activity Assay
  • 149药典 四部-2020 1200 Biological activity assay 1206 Cytochrome C activity assay
  • NY/T 2524-2013 Guidelines for the conduct of tests for distinctness, uniformity and stability - Button mushroom [Agaricus bisporus (J.E.Lange) Imbach]
  • 1133药典 化学药和生物制品卷-2010 Chapter 14 Antiallergic Drugs 3. Mast Cell Membrane Stabilizer Tranilast
  • 1132药典 化学药和生物制品卷-2010 Chapter 14 Antiallergic Drugs 3. Mast Cell Membrane Stabilizer Ketotifen Fumarate
  • 926兽药质量标准2017年版 Volume I of Biological Products Quality Standards for Veterinary Drugs Live Swine Fever Vaccine (Passed Cell Source)
  • 农业部1719号公告-1-2012 Live swine fever vaccine (passage cell source) (new veterinary drug registration) (three types)
  • 327药典 三部-2020 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
  • 274药典 四部-2020 3500 Biological activity-potency assay 3516 Anti-human T cell immunoglobulin potency assay (lymphocytotoxicity test)
  • 308药典 三部-2015 Biological Activity - Potency Assay 3526 Recombinant Human Granulocyte Macrophage Stimulating Factor Biological Activity Assay General Rules 135
  • 1131药典 化学药和生物制品卷-2010 Chapter 14 Antiallergic Drugs 3. Mast Cell Membrane Stabilizer Sodium Cromoglycate
  • 284药典 四部-2020 3500 Biological Activity-Potency Assay 3526 Recombinant Human Granulocyte Macrophage Stimulating Factor Biological Activity Assay
  • 247药典 三部-2010 Appendix Ⅹ XF Determination of Biological Activity of Recombinant Human Granulocyte Macrophage Stimulating Factor
  • 1155兽药质量标准2017年版 Biological Products Volume II Veterinary Drug Quality Standards Instructions for Live Swine Fever Vaccine (Passaging Cell Source)
  • 279药典 四部-2015 3500 Biological activity-potency assay 3516 Anti-human T cell immunoglobulin potency assay (lymphocytotoxicity test)
  • 337药典 三部-2020 Biological Activity-Potency Assay 3526 Human Granulocyte Macrophage Stimulating Factor Biological Activity Assay
  • 1134药典 化学药和生物制品卷-2010 Chapter 14 Antiallergic Drugs 3. Mast Cell Membrane Stabilizer Pimilulast Potassium

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)
  • DIN 58932-6 E:2021-02 Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes

国家市场监督管理总局、中国国家标准化管理委员会

  • GB/T 39729-2020 General requirements for measurement of cell purity—Flow cytometry
  • GB/T 39730-2020 General requirements for cell counting—Flow cytometry
  • GB/T 38484-2020 Determination of the biological activity for plant hormone-related secondary metabolites. Cytological method

Professional Standard - Aquaculture

Professional Standard - Pharmaceutical Packaging

Professional Standard - Hygiene

Professional Standard - Medicine

  • YY 0329-2002 Leukocyte removal filters for single use
  • YY 0329-2009 Leukocyte reduction filters for single use
  • 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/T 1251-2014 Erythrocyte sedimentation rate analyzer

Professional Standard - Commodity Inspection

  • SN/T 3824-2014 Phototoxicity test for cosmetics - Determination of recombinant red blood cell
  • SN/T 2242-2008 Natural killer cell activity assay

Professional Standard - Petrochemical Industry

  • SH/T 0680-1999 Heat transfer fluids - Determination of thermal stability

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

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

国家药监局

  • YY/T 1825-2021 Guideline for measurement uncertainty evaluation of the certified values using the erythrocytes and leucocytes reference measurement procedures

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 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 S91-142:1988 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 S91-143:1988 Dental implants. Cytocompatibility. Study of total cellular proteins.
  • NF S91-144:1988 Dental implants. Cytocompatibility. Evaluation of 51CR extracellular release.
  • NF U47-221:2010 Isolation on cell culture and identification by immunofluorescence of infectious haematopoietic necrosis virus of fish.
  • NF T90-387*NF EN 15972:2011 Water quality - Guidance on quantitative and qualitative investigations of marine phytoplankton.
  • NF S91-146:1988 Dental implants. Cytocompatibility. Study of cellular multiplication, migration and adherence.
  • 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 M60-220:2005 Radiation protection - Performance criteria for service laboratories performing biological dosimetry by cytogenetics.

KR-KS

  • KS M ISO 4590-2018 Rigid cellular plastics — Determination of the volume percentage of open cells and of closed cells

Korean Agency for Technology and Standards (KATS)

International Telecommunication Union (ITU)

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)
  • BS EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
  • BS EN ISO 21427-2:2006 Water quality. Evaluation of genotoxicity by measurement of the induction of micronuclei. Mixed population method using the cell line V79
  • BS ISO 19238:2004 Radiation protection - Performance criteria for service laboratories performing biological dosimetry by cytogenetics

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 19238:2017 Radiological protection - Performance criteria for service laboratories performing biological dosimetry by cytogenetics

SCC

  • 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 16418:2014 Paper and board — Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • AWWA ACE68896 Comparative Cytotoxicity and Genotoxicity of Priority DBPs
  • AWWA WQTC52850 Infectious Cryptosporidium parvum Detection by Cell Culture and PCR or Cell Culture and Antibodies?
  • 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
  • 12/30259424 DC BS EN 16418. Paper and board. Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
  • BS 1335:1946 Specification for air depolarized primary cells
  • BS 1335:1968 Specification for air depolarized primary cells
  • AWWA WQTC56953 Detection of Infectious Adenovirus by mRNA RT-PCR in Cell Culture
  • AS 2567:1982 Cytotoxic drug safety cabinets
  • AWWA WQTC52846 Comparison of Cell Culture and Animal Infectivity for Detection of Infectious Cryptosporidium parvum
  • 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
  • 12/30234846 DC BS ISO 19238. Radiation protection. Performance criteria for service laboratories performing biological dosimetry by cytogenetics
  • UNE 53201:1992 PLASTIC MATERIALS. FLEXIBLE FOAMS OF PUR. DETERMINATION OF NUMBER OF CELLS.
  • AS 2567:1994 Laminar flow cytotoxic drug safety cabinets

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

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 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
  • 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 EN 15845:2010-05 Paper and board - Determination of the cytotoxicity of aqueous extracts; German version EN 15845:2010
  • DIN 58932-6:2021-08 Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes; Text in German and English
  • DIN 40736-2:1992-06 Lead acid batteries; stationary cells with positive tubular plates; cells in hard-rubber containers; rated capacities, main dimensions, weights
  • 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

American Society for Testing and Materials (ASTM)

  • ASTM E2526-08 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 F1027-86(2007) Standard Practice for Assessment of Tissue and Cell Compatibility of Orofacial Prosthetic Materials and Devices
  • ASTM E2526-22 Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
  • ASTM D6226-21 Standard Test Method for Open Cell Content of Rigid Cellular Plastics
  • 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 F3206-17 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies
  • ASTM F3368-19 Standard Guide for Cell Potency Assays for Cell Therapy and Tissue Engineered Products

API - American Petroleum Institute

CU-NC

  • NC 90-13-43-1988 Standards System for Metrological Assurance. Determination of Cunductivity Cells Constant

American National Standards Institute (ANSI)

Lithuanian Standards Office

  • LST 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

Danish Standards Foundation

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

Military Standards (MIL-STD)

RU-GOST R

GB-REG

Standard Association of Australia (SAA)

  • AS 2282.11:1999 Methods for testing flexible cellular polyurethane - Determination of resilience

International Organization for Standardization (ISO)

  • ISO 19238:2004 Radiation protection - Performance criteria for service laboratories performing biological dosimetry by cytogenetics
  • ISO/DIS 24479:2023 Biotechnology — Cellular morphological analysis — General requirements and considerations for cell morphometry to quantify cell morphological features
  • ISO 19238:2014 Radiological protection - Performance criteria for service laboratories performing biological dosimetry by cytogenetics