Rules for dosing drugs in cell experiments
Rules for dosing drugs in cell experiments, Total:69 items.
The international standard classification for "Rules for dosing drugs in cell experiments" includes: Farming and forestry , Pesticides and other agrochemicals , Veterinary medicine .
The Chinese standard classification for "Rules for dosing drugs in cell experiments" includes: Pesticide management and application method , Animal quarantine, veterinary and epidemic prevention .
Professional Standard - Agriculture
- 农业部1247号公告-10-2009 Guiding principles for chromosomal aberration test of mouse bone marrow cells in veterinary drugs
- 986药典 化学药和生物制品卷-2010 Chapter 12 Antineoplastic Drugs Section 1 Cytotoxic Drugs 2. Drugs Affecting Nucleic Acid Synthesis Tegafur
- GB/T 43567-2023 Specification on general descriptors for cell-line resources
- NY/T 2186.4-2012 Microbial Pesticide Toxicological Test Guidelines - Part 4: Cell Culture Study
- 第3．1章OIE陆生动物诊断试验和疫苗手册-第七版 General guidelines - Laboratory methods for bacterial susceptibility testing
- NY/T 1386-2007 Principles of Good Laboratory Practice for Pesticide Physical-chemmical Testing
- 979药典 化学药和生物制品卷-2010 Chapter 12 Antineoplastic Drugs Section 1 Cytotoxic Drugs 2. Drugs Affecting Nucleic Acid Synthesis Cytarabine Hydrochloride
- 农业部1247号公告-12-2009 Guiding principles for micronucleus test in mouse bone marrow cells for veterinary drugs
Group Standards of the People's Republic of China
- T/SDHCST 006-2023 Procedures for Single Dose Toxicity Testing of the Cell Therapy Medical Products
- T/SHPPA 011-2021 Autologous CAR-T cell therapy medication supply chain management specifications
- T/SDHCST 005-2023 Procedures for Safety Pharmacology Testing of the Cell Therapy Medical Products
- T/QMHIPA 004-2022 Specification of Release Testing for Stem Cell-based Medicinal Products of Cell Preparation Center
- T/SHAAV 015-2024 Specifications for the construction of animal-derived bacterial resistance monitoring laboratories
- T/SHRH 027-2019 In Vitro Test -Inhibition of Melanin Synthesis in B16 Cells Test
- T/SDHCST 001-2023 General Principles on the Non-Clinical Studies of the Cell Therapy Medical Products
- T/CACM 1481-2023 Technical regulation of medicinal plant cell culture
- T/CALAS 86-2020 Laboratory animal-PCR method for detection of murine cytomegalovirus
- T/CRHA 003-2021 Laboratory-General requirements for testing of human-derived stem cell
- T/SDHCST 007-2023 Procedures for Repeated Dose Toxicity Testing of the Cell Therapy Medical Products
未注明发布机构
- DIN 12980 E:2015-08 Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs
- DIN 12980:1996 Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs
General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China
- GB/T 17980.37-2000 Pesticide - Guidelines for the field efficacy trials (I) - Nematocides against cyst nematode disease
- GB/T 15670.17-2017 Toxicological test methods for pesticides registration. Part 17: Mammalian spermatogonial/spermatocyte chromosome aberration test
Professional Standard - Commodity Inspection
- SN/T 1919-2007 Protocol of hemagglutination inhibition test for porcine parvovirus
American Society for Testing and Materials (ASTM)
- ASTM E1397-91(2003) Standard Practice for the in vitro Rat Hepatocyte DNA Repair Assay
- ASTM F1903-18 Standard Practice for Testing for Cellular Responses to Particles
in vitro - ASTM E1397-91(2008) Standard Practice for In Vitro Rat Hepatocyte DNA Repair Assay
- ASTM E1397-91(1998) Standard Practice for the in vitro Rat Hepatocyte DNA Repair Assay
- ASTM F1906-98 Standard Practice for Evaluation of Immune Responses In Biocompatibility Testing Using ELISA Tests, Lymphocyte, Proliferation, and Cell Migration
- ASTM F895-11(2016) Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
- 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 E1263-97(2003) Standard Guide for Conduct of Micronucleus Assays in Mammalian Bone Marrow Erythrocytes
- ASTM E2526-08 Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
- ASTM E2526-22 Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
- ASTM E1263-97 Standard Guide for Conduct of Micronucleus Assays in Mammalian Bone Marrow Erythrocytes
- ASTM E2526-08(2013) Standard Test Method for Evaluation of Cytotoxicity of Nanoparticulate Materials in Porcine Kidney Cells and Human Hepatocarcinoma Cells
HU-MSZT
- MSZ KGST 2702-1980 Laboratory diagnosis of yak leukocyte disease
SCC
- BS PAS 83:2006 Guidance on codes of practice, standardised methods and regulations for cell-based therapeutics
- DIN 12980 E:2015 Draft Document - Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs
- AAMI/ISO 13022:2012 Medical products containing viable human cells -- Application of risk management and requirements for processing practices
- DANSK DS/ISO 13022:2012 Medical products containing viable human cells - Application of risk management and requirements for processing practices
German Institute for Standardization
- DIN 12846:1978 Laboratory glassware; hematocrit capillaries
- DIN 12980:2016 Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs
- DIN 12980:2017 Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs
- 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 ISO 12772:2007-06 Laboratory glassware - Disposable microhaematocrit capillary tubes (ISO 12772:1997)
- DIN 12847-2:2000 Laboratory glassware - Haemacytometer counting chambers - Rulings
- DIN 12980:2005 Laboratory furniture - Safety cabinets for handling cytotoxic substances
- DIN 12847-1:1984 Laboratory glassware; haemacytometer counting chambers; general requirements
- DIN ISO 13022:2014-06 Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)
British Standards Institution (BSI)
- BS EN ISO 10993-5:1999 Biological evaluation of medical devices - Tests for in vitro cytotoxicity
- BS ISO 12772:1997(1999) Laboratory Glassware — Disposable microhaematocrit capillary tubes
- PD ISO/TR 10993-55:2023 Biological evaluation of medical devices. Interlaboratory study on cytotoxicity
GSO
- OS GSO ISO 12772:2010 Laboratory glassware -- Disposable microhaematocrit capillary tubes
- OS GSO ISO 13022:2016 Medical products containing viable human cells -- Application of risk management and requirements for processing practices
- GSO ISO 13022:2016 Medical products containing viable human cells -- Application of risk management and requirements for processing practices
Korean Agency for Technology and Standards (KATS)
- KS B ISO 12772-2021 Laboratory glassware－Disposable microhaematocrit capillary tubes
- KS B ISO 12772-2006(2016) Laboratory glassware－Disposable microhaematocrit capillary tubes
- KS B ISO 12772-2006(2021) Laboratory glassware－Disposable microhaematocrit capillary tubes
- KS P ISO 13022:2018 Medical products containing viable human cells — Application of risk management and requirements for processing practices
- KS P ISO 13022-2023 Medical products containing viable human cells — Application of risk management and requirements for processing practices
Standard Association of Australia （SAA）
- AS 2282.10:1999 Methods for testing flexible cellular polyurethane - Accelerated ageing tests
BE-NBN
- NBN-EN 304-1993 Heating boilers. Test code for heating boilers for atomizing oil burners
US-AAMI
- ANSI/AAMI/ISO 13022:2012 Medical products containing viable human cells.Application of risk management and requirements for processing practices
IX-FAO
- CAC/GL 40-1993(En) Pesticide Residue Analysis: A Guide to Good Laboratory Practice
- CAC/GL 40-1993,Rev.1-2003(Ch) Pesticide Residue Analysis: A Guide to Good Laboratory Practice
KR-KS
- KS P ISO 13022-2018(2023) Medical products containing viable human cells — Application of risk management and requirements for processing practices
Association Francaise de Normalisation
- NF EN ISO 17099:2018 Radioprotection - Performance criteria for laboratories carrying out biological dosimetry using the micronucleus test with blockade of cytodieresis (CBMN) in peripheral blood lymphocytes
