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Cytotoxicity

Cytotoxicity, Total:71 items.

In the international standard classification, Cytotoxicity involves: Air quality, Occupational safety. Industrial hygiene, Water quality, Materials and articles in contact with foodstuffs, Packaging materials and accessories, Microbiology, Analytical chemistry, Laboratory medicine, Medical equipment, Sterilization and disinfection, Products of the chemical industry, Paper and board, Dentistry, Medical sciences and health care facilities in general.

Professional Standard - Pharmaceutical Packaging, Cytotoxicity

YBB 0001-2003 Xibao Duxing Jianchafa Tests for cytotoxicity
YBB 0001(03)-2003 Cytotoxicity Test (Trial)

Standard Association of Australia （SAA）, Cytotoxicity

AS 2567:2002 Laminar flow cytotoxic drug safety cabinets
AS 2252.5:2017 Controlled environments, Part 5: Cytotoxic drug safety cabinets (CDSC) — Design, construction, installation, testing and use
AS 1807:2021 Separative devices — Biological and cytotoxic drug safety cabinets, clean workstations and pharmaceutical isolators — Methods of test

European Committee for Standardization (CEN), Cytotoxicity

EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
EN ISO 10993-5:2009 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)
EN ISO 10993-5:1999 Biological Evaluation of Medical Devices - Part 5: Tests for In Vitro Cytotoxicity ISO 10993-5:1999; Supersedes EN 30993-5:1994

Danish Standards Foundation, Cytotoxicity

DS/EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
DS/EN 30993-5:1994 Biological evaluation of medical devices-Part 5:Tests for cytotoxicity-in vitro methods

Lithuanian Standards Office , Cytotoxicity

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

AENOR, Cytotoxicity

UNE-EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
UNE-EN ISO 10993-5:2009 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
UNE-EN 16418:2014 Paper and board - Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)

German Institute for Standardization, Cytotoxicity

DIN EN 15845:2010-05 Paper and board - Determination of the cytotoxicity of aqueous extracts; German version EN 15845:2010
DIN 12980:2005 Laboratory furniture - Safety cabinets for handling cytotoxic substances
DIN EN ISO 10993-5:2009-10 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009); German version EN ISO 10993-5:2009
DIN EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts; German version EN 15845:2010
DIN 12980:2017 Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs
DIN 12980:2016 Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs
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 12980:2017-05 Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs / Note: DIN 12980 (2005-06) remains valid alongside this standard until 2017-04-01.
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

Association Francaise de Normalisation, Cytotoxicity

NF EN 15845:2010 Papier et carton - Détermination de la cytotoxicité des extraits aqueux
NF Q03-098*NF EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
NF EN ISO 10993-5:2010 Évaluation biologique des dispositifs médicaux - Partie 5 : essais concernant la cytotoxicité in vitro
NF S99-501-5*NF EN ISO 10993-5:2010 Biological evaluation of medical devices - Part 5 : tests for in vitro cytotoxicity.
NF EN 16418:2014 Papier et carton - Détermination de l'effet cytotoxique d'extraits aqueux en utilisant une lignée cellulaire d'hépatome possédant des enzymes du métabolisme (cellules HepG2)
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 S99-505:1994 BIOLOGICAL EVALUATION OF MEDICAL DEVICES. PART 5 : TESTS FOR CYTOTOXICITY : IN VITRO METHODS. (EUROPEAN STANDARD EN 30993-5).

American Society for Testing and Materials (ASTM), Cytotoxicity

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 E2526-22 Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
ASTM E1482-23 Standard Practice for Use of Gel Filtration Columns for Cytotoxicity Reduction and Neutralization
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 E2526-08 Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells

British Standards Institution (BSI), Cytotoxicity

BS EN 15845:2010 Paper and board - Determination of the cytotoxicity of aqueous extracts
BS EN ISO 10993-5:1999 Biological evaluation of medical devices - Tests for in vitro cytotoxicity
PD ISO/TR 10993-55:2023 Biological evaluation of medical devices. Interlaboratory study on cytotoxicity
BS ISO 19007:2018 Nanotechnologies. In vitro MTS assay for measuring the cytotoxic effect of nanoparticles
BS EN ISO 10993-5:2009 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
BS EN 16418:2014 Paper and board. Determination of the cytotoxicity of aqueous extracts using a metabolically competent hepatoma cell line (HepG2)

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

GB/T 41915-2022 Nanotechnologies—In vitro MTS assay for measuring the cytotoxic effect of nanoparticles
GB/T 16886.5-2017 Biological Evaluation of Medical Devices Part 5: In Vitro Cytotoxicity Tests
GB/T 16886.5-2003 Biological evaluation of medical devices--Part 5: Test for in vitro cytotoxicity

Professional Standard - Agriculture, Cytotoxicity

315药典四部-2020 4000 Testing method for pharmaceutical packaging materials 4014 Cytotoxicity testing method for pharmaceutical packaging materials

Taiwan Provincial Standard of the People's Republic of China, Cytotoxicity

CNS 14393-5-2004 Biological evaluation of medical devices – Part 5：Tests for in vitro cytotoxicity
CNS 14393.5-2004 Biological evaluation of medical devices – Part 5：Tests for in vitro cytotoxicity

VN-TCVN, Cytotoxicity

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

TH-TISI, Cytotoxicity

TIS 2395.5-2008 Biological evaluation of medical devices.part 5: tests for in vitro cytotoxicity

ZA-SANS, Cytotoxicity

SANS 10993-5:2003 Biological evaluation of medical devices Part 5: Tests for in vitro cytotoxicity

American National Standards Institute （ANSI), Cytotoxicity

ANSI/AAMI/ISO 10993-5:2009 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity

PH-BPS, Cytotoxicity

PNS ISO 19007:2021 Nanotechnologies - In vitro MTS assay for measuring the cytotoxic effect of nanoparticles
PNS ISO 10993-5:2021 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity

International Organization for Standardization (ISO), Cytotoxicity

ISO 10993-5:1999 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity
ISO 19007:2018 Nanotechnologies — In vitro MTS assay for measuring the cytotoxic effect of nanoparticles
ISO 10993-5:1992 Biological evaluation of medical devices — Part 5: Tests for cytotoxicity: in vitro methods
ISO 10993-5:2009 Biological evaluation of medical devices — Part 5: Tests for cytotoxicity: in vitro methods
ISO/TR 10993-55:2023 Biological evaluation of medical devices — Part 55: Interlaboratory study on cytotoxicity

Korean Agency for Technology and Standards (KATS), Cytotoxicity

KS P ISO 10993-5:2018 Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity

KR-KS, Cytotoxicity

KS P ISO 10993-5-2018 Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity

Professional Standard - Medicine, Cytotoxicity

YY/T 0127.18-2016 Biological evaluation of medical devices used in dentistry.Part 18:Dentine barrier cytotoxicity test
YY/T 0993-2015 Biological evaluation of medical devices.Nanomaterial: In vitro cytotoxicity tests (MTT assay and LDH assay)

RU-GOST R, Cytotoxicity

GOST ISO 10993-5-2011 Medical devices. Biological evaluation of medical devices. Part 5. Tests for in vitro cytotoxicity
GOST R ISO 10993.5-1999 Medical devices. Biological evaluation of medical devices. Part 5. Tests for cytotoxicity: in vitro methods

Professional Standard - Public Safety Standards, Cytotoxicity

GA/T 2056-2023

BE-NBN, Cytotoxicity

NBN-EN 30993-5-1994 Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992)

RO-ASRO, Cytotoxicity

STAS SR EN 30993-5-1996 Biological evaluation of medical devices -Part 5: Tests for cytotoxicity: in vitro methods

Canadian Standards Association (CSA), Cytotoxicity

CSA Z316.6-02-2002 Evaluation of Single Use Medical Sharps Containers for Biohazardous and Cytotoxic Waste Second Edition