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SN/T 2285-2009: Good laboratory practice for cosmetics alternative testing in vitro
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| Standard ID | Contents [version] | USD | STEP2 | [PDF] delivered in | Standard Title (Description) | Status | PDF |
| SN/T 2285-2009 | English | 369 |
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Good laboratory practice for cosmetics alternative testing in vitro
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SN/T 2285-2009
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Basic data | Standard ID | SN/T 2285-2009 (SN/T2285-2009) | | Description (Translated English) | Good laboratory practice for cosmetics alternative testing in vitro | | Sector / Industry | Commodity Inspection Standard (Recommended) | | Classification of Chinese Standard | Y42 | | Classification of International Standard | 71.100.70 | | Word Count Estimation | 14,183 | | Date of Issue | 2009-02-20 | | Date of Implementation | 2009-09-01 | | Quoted Standard | GB/T 27025-2008; GB 19489; ISO 15190-2003 | | Regulation (derived from) | National Quality Inspection [2009] No. 67 | | Issuing agency(ies) | General Administration of Customs | | Summary | This standard specifies the safety evaluation in the cosmetics vitro toxicology tests, the laboratory shall comply with good practice. This standard applies to raw materials and products in cosmetic safety evaluation of toxicological animal alternative testing laboratories. This standard also applies in the food and its additives, contact materials, chemical raw materials and products of animal safety evaluation of alternative toxicological research and testing laboratories. | SN/T 2285-2009: Good laboratory practice for cosmetics alternative testing in vitro---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Good laboratory practice for cosmetics alternative testing in vitro
Exit inspection and quarantine industry standard book People's Republic of China
In vitro alternatives Cosmetics Laboratory Practice
Posted 2009-02-20
2009-09-01 implementation
People's Republic of China
The State Administration of Quality Supervision, Inspection and Quarantine released
Foreword
This standard is proposed and managed by the National Certification and Accreditation Administration Committee.
This standard was drafted. People's Republic of China Guangdong Entry-Exit Inspection and Quarantine Beijing People's Republic of China
Bureau, Chinese Academy of Inspection and Quarantine.
The main drafters of this standard. Jiao Hong, Cheng Shujun, Lin Li, Yang Jing, Ma Guiping, Dong Yiyang.
This standard is the first release of the entry-exit inspection and quarantine industry standards.
In vitro alternatives Cosmetics Laboratory Practice
1 Scope
This standard specifies the time in cosmetics in vitro toxicological safety evaluation test, the laboratory shall comply with good practice.
This standard applies to the safety of cosmetic ingredients in the product and toxicological evaluation of alternative animal testing laboratories.
This standard also applies in food additives and contact materials, safety of chemical raw materials and products of animal toxicology evaluation of alternatives
Research and testing laboratories.
2 Normative references
The following documents contain provisions which, through reference in this standard and become the standard terms. For dated references, subsequent
Amendments (not including errata content) or revisions do not apply to this standard, however, encourage the parties to the agreement are based on research
Whether the latest versions of these documents. For undated reference documents, the latest versions apply to this standard.
GB/T 27025-2008 testing and calibration laboratories General requirements (ISO 17025.2005, IDT)
GB 19489 General requirements for laboratory biosafety
ISO 15190.2003 Safety requirements for medical laboratories
3 Terms and Definitions
The following terms and definitions apply to this standard.
3.1
The use of live animals or biological tests carried out.
3.2
Test cell or tissue in vitro carried out.
3.3
Improve trial design and improve test efficiency to reduce animal stress (alternative optimization), reducing the number of animals required for a test (decrease
Substitution), and a complete cessation of the use of animals in research trials (instead of substitution), and to achieve the object of the.
3.4
The use of lower animals or the use of isolated organs, cultured cells or organelles, biological simulation system to optimize, reduce or replace traditional fixed
Experiments were carried out toxicological evaluation, efficacy evaluation and other life sciences research.
3.5
Application of the principle of life science research in animal testing should follow generally means reducing the number of animal experiments, optimization of existing animal test side
And the development of new methods to replace animal testing technology, as well as the efforts and measures to achieve the above object made.
3.6
The laboratory test planning, execution, monitoring, recording, reporting and organizational processes and conditions archives quality management system.
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