Pharmaceutical company passes GSP flight inspection
Release time:
2020-09-01
Pharmaceutical Company Passed GSP Flight Inspection
News In order to standardize the operation behavior of drug wholesale and retail links, strengthen the prevention and control of safety risks, and ensure the quality and safety of drug use and legitimate rights and interests of the public, according to the "Jinhua City 2020 Annual Flight Inspection Implementation Plan for Drug Wholesale Enterprises (Retail Chain Headquarters), 7# August 29 -31 , Jinhua Drug Certification and Inspection Center conducted a three-day flight inspection of Jinhua Pharmaceutical Company.
The inspection team inspected the pharmaceutical company's quality management system, personnel management files, personnel qualification and drug business and sales processes, etc., and focused on the on-site management of the warehouse, storage conditions, drug (material) storage quality, and employee position The operation process was randomly checked, in particular, special drugs such as essence, hemp, poison and release have been strictly and meticulously inspected from procurement to storage to sales and capital return. The final inspection team believes that the quality management system of Jinhua Pharmaceutical Company is basically in line with sound, complete facilities and equipment and normal operation, basically meeting the requirements of management and quality control in the whole process of operation, and the responsibilities of personnel in each post are basically clear and familiar with the post operation procedures. the procurement and acceptance, storage, sales management and after-sales management of drugs are basically standardized, and the management and control of special drugs meet the requirements. The inspection team put forward correction requirements for the problems found in the inspection to effectively ensure the quality and safety of drug trading and storage. Wu Weisheng, general manager ofPharmaceutical Company, said that the quality management of pharmaceutical business is the top priority of pharmaceutical companies. Through careful and detailed inspection and guidance by the inspection team, the quality management procedures of enterprises can be standardized and the quality management level of enterprises can be improved. Pharmaceutical companies will take this GSP
flight inspection as an opportunity to further strengthen the whole process of enterprise quality management and employee job skills training, enhance employees' awareness of drug quality management, strengthen on-site supervision and inspection of storage departments, and effectively ensure the quality of drug storage, Ensure the quality and safety of public drug use, and assume the social responsibility of enterprises. (Fan Tufa)
More information
Publicity of Environmental Protection Acceptance for Completion of Kiln End Flue Gas Desulfurization Project of daye peak cement co., ltd. According to the requirements of the Interim Measures for Environmental Protection Acceptance for Completion of Construction Projects (No.4 [2017] of the State Environmental Regulations) issued by the Ministry of Environmental Protection, the environmental protection acceptance information of "Kiln End Flue Gas Desulfurization Project" of daye peak cement co., ltd. is now publicized. Basic Information of 1. Project Project Name: Kiln End Flue Gas Desulfurization Project Construction Unit: daye Jianfeng Cement Co., Ltd. Project Construction Location: Yongguang Village, Baoan Town, daye city, nature of the project in the existing plant area of daye Jianfeng Cement Co., Ltd.: The construction content of the technological transformation project is: This technological transformation project is mainly to build a wet desulfurization system for kiln end gas of the company's existing 4000t cement clinker production line, adopting limestone-gypsum wet flue gas desulfurization process. The project covers a total area of 500 m2, with a new construction area of about 450 m2. It mainly builds desulfurization complex building, flue gas system, SO2 absorption system, limestone powder conveying and limestone slurry preparation system, process water system, gypsum dehydration system and supporting pipelines. Power supply, water supply, compressed air and other public works rely on the existing plant. Total investment and environmental protection investment: the total investment of the project is 10.37 million yuan, all of which are environmental protection investment. The project was entrusted to Huangshi Yangtze River Environmental Engineering Design and Research Institute to carry out environmental impact assessment in September 2017. On November 16, 2017, Daye Municipal Environmental Protection Bureau issued a reply with YEHAN [2017] No. 354. Implementation of 2. environmental protection measures The scope of this acceptance is the flue gas desulfurization system and supporting facilities at the end of the kiln. (1) Exhaust gas pollution
2020
07-31
Spike New Drug Approved for Registration
On April 16, Jianfeng Pharmaceutical Company received the approval and issuance of Olopatadine Hydrochloride Eye Drops "Drug Registration Approval" (approval number: 2019S00296) approved by the State Drug Administration. Olopatadine hydrochloride eye drops is mainly used to treat the signs and symptoms of allergic conjunctivitis. It is a mast cell stabilizer and a relatively selective histamine H1-receptor antagonist. It can inhibit type I immediate allergic reactions in vivo and in vitro experiments. At present, the product has been included in the "National Basic Medical Insurance, Work Injury Insurance and Maternity Insurance Drug Catalog (2017 Edition)" and classified as Class B. According to the relevant data of IMS database, in 2018, the global sales of olopatadine hydrochloride eye drops were about 0.37 billion US dollars, and the sales in China were about 10.232 million US dollars. Spike Pharmaceuticals already has the corresponding production line, this time to obtain the registration approval, marking Spike Pharmaceuticals has the qualification to carry out the production and sales of olopatadine hydrochloride eye drops, will further enrich the product line of Spike Pharmaceuticals, help to enhance the competitiveness of the company's pharmaceutical business. (Xia Yingpin)
2020
07-31
Spike New Drug Approved for Registration
On April 16, Jianfeng Pharmaceutical Company received the approval and issuance of Olopatadine Hydrochloride Eye Drops "Drug Registration Approval" (approval number: 2019S00296) approved by the State Drug Administration. Olopatadine hydrochloride eye drops is mainly used to treat the signs and symptoms of allergic conjunctivitis. It is a mast cell stabilizer and a relatively selective histamine H1-receptor antagonist. It can inhibit type I immediate allergic reactions in vivo and in vitro experiments. At present, the product has been included in the "National Basic Medical Insurance, Work Injury Insurance and Maternity Insurance Drug Catalog (2017 Edition)" and classified as Class B. According to the relevant data of IMS database, in 2018, the global sales of olopatadine hydrochloride eye drops were about 0.37 billion US dollars, and the sales in China were about 10.232 million US dollars. Spike Pharmaceuticals already has the corresponding production line, this time to obtain the registration approval, marking Spike Pharmaceuticals has the qualification to carry out the production and sales of olopatadine hydrochloride eye drops, will further enrich the product line of Spike Pharmaceuticals, help to enhance the competitiveness of the company's pharmaceutical business. (Xia Yingpin)
2020
07-31
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