GB/T 22275.4-2008 English PDFUS$174.00 ยท In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. GB/T 22275.4-2008: Requirements of conduct for Good Laboratory Practice (GLP) -- Part 4: The application of the GLP principles to field studies Status: Valid
Basic dataStandard ID: GB/T 22275.4-2008 (GB/T22275.4-2008)Description (Translated English): Requirements of conduct for Good Laboratory Practice (GLP) -- Part 4: The application of the GLP principles to field studies Sector / Industry: National Standard (Recommended) Classification of Chinese Standard: A00 Classification of International Standard: 03.120.20 Word Count Estimation: 9,920 Date of Issue: 2008-08-04 Date of Implementation: 2009-04-01 Quoted Standard: GB/T 22275.1; GB/T 22278-2008 Adopted Standard: OECD GLP, IDT; ENVJMMONO (99)22, IDT Regulation (derived from): Announcement of Newly Approved National Standards No. 12 of 2008 (No. 125 overall) Issuing agency(ies): General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China, Standardization Administration of the People's Republic of China Summary: This standard specifies the on-site research and test organization organization and personnel, quality assurance programs, test facilities, equipment, raw materials, reagents, test systems, test and reference samples, standard operating procedures, the findings of the report, recording and storage of materials and reservations. Except as expressly exempted from national legislation, under this Part Laboratory Practice applies to and regulations as required all non-clinical health and environmental safety studies, including pharmaceuticals, pesticides, food additives and feed additives, cosmetics, veterinary drugs and similar products Registration or apply for a license, and industrial chemicals management. GB/T 22275.4-2008: Requirements of conduct for Good Laboratory Practice (GLP) -- Part 4: The application of the GLP principles to field studies---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. Requirements of conduct for Good Laboratory Practice (GLP). Part 4. The application of the GLP principles to field studies ICS 03.120.20 A00 National Standards of People's Republic of China Good laboratory specification implementation requirements Part 4. Good Laboratory Practice Principles are on site Research application 2008-08-04 released 2009-04-01 implementation General Administration of Quality Supervision, Inspection and Quarantine of People's Republic of China China National Standardization Administration released ForewordGB/T 22275 "good laboratory practice requirements" is divided into seven parts. --- Part 1. Quality Assurance and Good Laboratory Practice; --- Part 2. Tasks and responsibilities of project leaders in good laboratory norms; --- Part 3. laboratory suppliers on the principles of Good Laboratory Compliance; --- Part 4. Principles of good laboratory norms in the field of research applications; --- Part 5. good laboratory norms in the application of short-term research; --- Part 6. The application of good laboratory norms in computerized systems; --- Part 7. Good Laboratory Practice Principles in the organization and management of multi-site research applications. This section GB/T 22275 Part 4. This section identical with the Organization for Economic Co-operation and Development (OECD) Good Laboratory Practice (GLP) principles and compliance monitoring series of documents No. 6. "The Application of GLP Principles in Field Research" [ENV/JM/MONO (99) 22]. This section made the following editorial changes. --- Remove the foreword and directory section. This part of the National Standardization Technical Committee for the management of hazardous chemicals (SAC/TC251) proposed and managed. This part of the drafting unit. Exit Inspection and Quarantine of Shandong. The main drafters of this section. Wan Min, yellow safflower, He Fei, Wang Xiaobing, Wang Huiyong. Good laboratory specification implementation requirements Part 4. Good Laboratory Practice Principles are on site Research application1 ScopeGB/T 22275 provisions of this part of the field research organizations and personnel testing organizations, quality assurance programs, test facilities, equipment, Materials, reagents, test systems, test samples and references, standard operating procedures, reports of findings, records and storage and retention of materials. In addition to the explicit exemptions from national legislation, the Good Laboratory Practice Principles (hereinafter referred to as GLP Principles) as set forth in this section apply to laws and regulations All required non-clinical health and environmental safety studies, including medicines, pesticides, food additives and feed additives, cosmetics, veterinary drugs and Registration of similar products or application for permits, and management of industrial chemicals.2 Normative referencesThe following documents contain provisions that, through the reference in this part of GB/T 22275, become the provisions of this section. Any reference to the date of the citation All subsequent amendments (not including errata content) or revisions do not apply to this section, however, encouraged to be reached under this section The parties to the agreement examine whether the latest versions of these documents are available. For undated references, the latest version applies to this book section. GB/T 22275.1 Good Laboratory Practice requirements Part 1. Quality Assurance and Good Laboratory Practice GB/T 22278-2008 Principles of Good Laboratory Practice3 Terms and definitionsGB/T 22278-2008 Terms and definitions apply to this section.4 main technical specifications4.1 Background In 1981, the Organization for Economic Co-operation and Development (OECD) adopted the GLP principles. In.1997, the OECD revised it. GLP original Recommended test management standards are provided for a variety of studies for management purposes or for other purposes related to evaluation. The 1981 GLP original The OECD panel made clear in its reports the types of tests covered by the GLP principles. a) Physical and chemical properties; b) Toxicology studies (long-term and short-term) for evaluating the health effects on humans; c) Ecotoxicological studies (long-term and short-term) to evaluate environmental effects; d) Ecological studies (transport, biodegradation and bioaccumulation) for assessing the environmental fate of chemicals. The general classification of ecological studies also includes those used for the determination of residual pesticides, metabolites and for drug resistance and other dietary exposures Test of the characteristics and quantity of his compounds. GLP principles are used to cover more chemical products, including pesticides, pharmaceuticals, cosmetics, veterinary drugs, food Additives, feed additives, industrial chemicals. Oversight authorities in OECD member countries have received most of the GLP compliance oversight in the area of (non-clinical) toxicology testing Test This is because these studies are traditionally considered to be the most important from a human health point of view. Many of the OECD member countries have been established Compliance monitoring programs have evolved from the experience gained with toxicology laboratory tests. Laboratory character of ecotoxicological research Integrity monitoring procedures have also been well developed. Research programs, conditions, methods, techniques and developments in field studies of pesticides or veterinary drugs (eg residue studies, metabolic studies and ecological studies) ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of GB/T 22275.4-2008_English be delivered?Answer: Upon your order, we will start to translate GB/T 22275.4-2008_English as soon as possible, and keep you informed of the progress. 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