SB/T 11037-2013 English PDF
Basic dataDetail Information of SB/T 11037-2013; SB/T11037-2013Description (Translated English): Service specification pharmaceutical commerce enterprises of medical institutions Sector / Industry: Domestic Trade Industry Standard (Recommended) Classification of Chinese Standard: C00 Classification of International Standard: 03.080.20 Word Count Estimation: 13,141 Date of Issue: 2013-12-04 Date of Implementation: 2014-06-01 Quoted Standard: GB/T 28842-2012; SB/T 10767-2012 Drafting Organization: China Pharmaceutical Business Association Administrative Organization: People's Republic of China Ministry of Commerce Regulation (derived from): No. 8 of 2014 (No. 176) China Industry Standards Record Announcement Proposing organization: PRC Ministry of Commerce Issuing agency(ies): PRC Ministry of Commerce Summary: This standard stipulates the service items of medical commercial enterprises to medical institutions and their contents, as well as the standards that should be met by the service and the supervision and evaluation of service quality, and proposes the organizations, facilities and personnel that pharmaceutical commercial enterprises should have in order to do a good job. Requirements. This standard applies to pharmaceutical commercial enterprises within the territory of the People's Republic of China and to pharmaceutical manufacturers that sell pharmaceutical products directly to hospitals. SB/T 11037-2013: Service specification pharmaceutical commerce enterprises of medical institutions---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. Service specification pharmaceutical commerce enterprises of medical institutions ICS 03.080.20 C00 Record number. 46957-2014 People's Republic of China domestic trade industry standard Service specification of medical commercial enterprises to medical institutions Released on.2013-12-04 2014-06-01 implementation Published by the Ministry of Commerce ForewordThis standard is a recommended industry standard, based on the "Contract Law of the People's Republic of China", "The Drug Administration Law of the People's Republic of China" Quality Management Regulations, based on the development status of the domestic pharmaceutical circulation industry, with reference to the development level of the pharmaceutical circulation industry in developed countries, comprehensive above The factors are formulated; the purpose is to promote the standardization and standardization of medical business enterprises' services to medical institutions, and to comprehensively improve the sales of medical products. Distribution and supply service work quality. This standard was drafted in accordance with the rules given in GB/T 1.1-2009. This standard is proposed and managed by the Ministry of Commerce of the People's Republic of China. This standard was drafted. China Pharmaceutical Business Association, Sinopharm Holding Co., Ltd., China Resources Pharmaceutical Commercial Group Co., Ltd., Guangzhou Medical Pharmaceutical Co., Ltd., Chongqing Pharmaceutical (Group) Co., Ltd., Zhejiang Yingte Pharmaceutical Co., Ltd., Huadong Pharmaceutical Co., Ltd., Yunnan Provincial Pharmaceutical Co., Ltd. Service specification of medical commercial enterprises to medical institutions1 ScopeThis standard stipulates the service items of medical commercial enterprises to medical institutions and their contents, as well as the standards and standards for services. The supervision and evaluation of service quality puts forward the requirements of the organizations, facilities and personnel that pharmaceutical commercial enterprises should have in order to do a good job. This standard applies to pharmaceutical commercial enterprises within the territory of the People's Republic of China and to pharmaceutical manufacturers that sell pharmaceutical products directly to hospitals.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 28842-2012 Pharmaceutical cold chain logistics operation specification SB/T 10767-2012 Evaluation index of logistics service capacity of pharmaceutical wholesale enterprises3 Terms and definitionsThe following terms and definitions apply to this document. 3.1 Medical commodity themedicinecommodity Special commodities for preventing and treating various diseases, ensuring good health and conducting scientific experiments are to save lives, save lives, and analyze and test. Necessities, including drugs (referring to chemicals), medical devices, chemical reagents, glass instruments, proprietary Chinese medicines, and Chinese herbal medicines. 3.2 Drug drug For the prevention, treatment, diagnosis of human diseases, purposefully regulate the physiological functions of the human body and provide indications or indications for function, use and use Amount of substances, including Chinese herbal medicines, Chinese herbal medicines, Chinese patent medicines, chemical raw materials and their preparations, antibiotics, biochemical drugs, radioactive drugs, serum, Vaccines, blood products and diagnostic drugs. [Drug Administration Law, Article 102] 3.3 Specially managed drug drugunderspecialmanagement Including narcotic drugs, psychotropic drugs, medical toxic drugs, radioactive drugs. 3.4 Refrigerated drug coldstoragedrug For the storage and transportation of drugs with cold, freezing and other temperature requirements. [GB/T 28842-2012, definition 3.1] 3.5 Pharmaceutical business enterprise pharmaceuticalcommerceenterprises Enterprises engaged in the operation of pharmaceutical commodities; among them, those engaged in the operation of pharmaceuticals and medical devices refer to the "pharmaceutical business license" and "drugs". Management Quality Management Standard Certificate "Medical Device Business Enterprise License" (limited to second-class and third-class medical device enterprises) The Legal Person Business License, which sells pharmaceutical products such as medicines and medical devices purchased to pharmaceutical commodity manufacturers, business enterprises and medical institutions. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of SB/T 11037-2013_English be delivered?Answer: Upon your order, we will start to translate SB/T 11037-2013_English as soon as possible, and keep you informed of the progress. 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