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Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. RB/T 193-2015: Guidance for the application of good laboratory practice for peer review of histopathology Status: Valid
Basic dataStandard ID: RB/T 193-2015 (RB/T193-2015)Description (Translated English): Guidance for the application of good laboratory practice for peer review of histopathology Sector / Industry: Chinese Industry Standard (Recommended) Classification of Chinese Standard: A00 Classification of International Standard: 03.120.20 Word Count Estimation: 9,914 Date of Issue: 2015-12-17 Date of Implementation: 2016-07-01 Quoted Standard: GB/T 22278-2008 Regulation (derived from): State-Accreditation-Science (2015)77 Issuing agency(ies): National Certification and Accreditation Administration Summary: This International Standard specifies the use of the GLP principle in peer review of histopathology and provides guidelines for the pathophysiology peer review of pathologists, test facility managers, project leaders, and quality assurance personnel. This standard applies to all non-clinical health and environmental safety studies required by regulation, including registration or licensing of pharmaceuticals, pesticides, food additives and feed additives, cosmetics, veterinary drugs and similar products, and industrial chemicals management. RB/T 193-2015: Guidance for the application of good laboratory practice for peer review of histopathology---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. Guidance for the application of good laboratory practice for peer review of histopathology ICS 03.120.20 A00 People's Republic of China certification and recognition of industry standards Good laboratory practices in histopathology Application Guide in Peer Review Histopathology Released on.2015-12-17 2016-07-01 implementation China National Certification and Accreditation Administration issued ForewordThis standard was drafted in accordance with the rules given in GB/T 1.1-2009. This standard was proposed by the China National Accreditation Center for Conformity Assessment. This standard is under the jurisdiction of the National Certification and Accreditation Standardization Technical Committee (SAC/TC261). This standard was drafted. China National Accreditation Center for Conformity Assessment, China National Institute for Food and Drug Control, National Drug Safety Evaluation and Monitoring Xin, Institute of New Drug Safety Evaluation, Peking Union Medical College, Chinese Academy of Medical Sciences, Institute of Chemical Safety, China Academy of Inspection and Quarantine. The main drafters of this standard. Wu Xiaoyu, Lu Jianjun, Wang Aiping, Wei Jinfeng, Li Haishan, Cao Shi, Han Chunxu.IntroductionThis standard refers to the Organization for Economic Cooperation and Development (Organization for Economic Cooperation and Development, OECD) GoodLaboratory Practice (GLP) Principles and Compliance Monitoring Series Document No. 16 Application Guidelines for Laboratory Standards in Pediatric Peer Review [OECDENV/JM/MONO (2014) 30]. Good laboratory practices in histopathology Application Guide in Peer Review1 ScopeThis standard gives the application of the GLP principle in the peer review of histopathology, and is responsible for pathologists, test institution managers, and projects. Human and quality assurance personnel provide guidance on peer-reviewed histopathology. This standard applies to all non-clinical health and environmental safety studies required by regulations, including medicines, pesticides, food additives and feed. Registration or application for additives, cosmetics, veterinary drugs and similar products, as well as industrial chemicals management.2 Normative referencesThe following documents are indispensable for the application of this document. For dated references, only the dated version applies to this article. Pieces. For undated references, the latest edition (including all amendments) applies to this document. GB/T 22278-2008 Good Laboratory Practice Principles3 Terms and definitionsThe terms and definitions defined in GB/T 22278-2008 apply to this document.4 Main technical specifications4.1 Background Pathological evaluation of tissue samples is an important part of toxicity studies, and pathological evaluation results are crucial for toxicity studies. The evaluation of the tissue sample is based on the professional opinion of the reading pathologist. The peer review by the testing organization is usually another disease. The physiologist reads the pieces of the tissue. This guide ensures the quality and accuracy of professional advice and regulates peer review. Although at There is no clear provision for peer review in the GLP principles given in GB/T 22278-2008, but most research data acceptance departments still It is hoped that the results of histopathological diagnosis will be peer-reviewed to some extent. This guide focuses on the organization, implementation, and documentation of peer review. The result of the program. Peer review may result in changes in histopathological findings and reported results, which may alter research findings and conclusions. This standard To provide guidance to pathologists, test facility managers, project leaders, and quality assurance personnel in the implementation of histopathology How to plan, manage, record and report in peer review to comply with GLP principles. Specific implementation of peer-reviewed histopathology can be Refer to Section 3.6.3.7 of the OECD Test and Evaluation Series Document No. 116 (Appendix A). For some special research projects, the client may require some or all of the histopathological sections to be peer-reviewed by a special pathologist. Negotiation. The pathologist who participated in the review may be a well-known expert in the field of specific pathophysiology, or a physiological effect on the study of the test substance. Have specialized experience. This ensures that the effects of the same test in different studies are consistent in terminology and interpretation. Due to phase Experts are not necessarily employed by GLP testing facilities, so it is not possible for all peer review to be implemented in the same GLP institution. 4.2 Application of GLP Principles 4.2.1 Any information that is peer-reviewed within the testing organization or peer-reviewed by an external consultant, in a research plan or plan ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of RB/T 193-2015_English be delivered?Answer: Upon your order, we will start to translate RB/T 193-2015_English as soon as possible, and keep you informed of the progress. The lead time is typically 1 ~ 3 working days. 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