SN/T 2285-2009 English PDF

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SN/T 2285-2009: Good laboratory practice for cosmetics alternative testing in vitro
Status: Valid

Standard ID	USD	BUY PDF	Lead-Days	Standard Title (Description)	Status
SN/T 2285-2009	369	Add to Cart	3 days	Good laboratory practice for cosmetics alternative testing in vitro	Valid

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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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