Congratulations on the cooperation between Nanchang Feihong pharmaceutical and our company
Nanchang Feihong Pharmaceutical Co., Ltd., established in 1993, is located in the pharmaceutical port of Nanchang national high tech Industrial Development Zone, and is one of the major pharmaceutical manufacturers introduced by Nanchang national high tech Industrial Development Zone. The second phase of the project under construction includes two tablet workshops with three production lines, and the new dosage forms include granules, etc. At present, the main products are oyster calcium carbonate bulk drug, oyster calcium carbonate chewable tablets, ferrous lactate tablets and nimesulide dispersible tablets, metformin hydrochloride sustained-release tablets, etc. Among them, ferrous lactate tablet is the national product; nimesulide dispersible tablet has obtained the certificate of high and new technology product; one class II new drug "rifaximin raw material and tablet" which has obtained the production approval; one class III new drug "balofloxacin tablet and raw material" which has obtained the clinical approval; one class III new drug "compound pseudoephedrine hydrochloride sustained release tablet" which has completed the clinical trial of the drug to be reported for production; and the national drug The products to be approved by the evaluation center include indapamide tablets, acyclovir dispersible tablets, clarithromycin dispersible tablets, amoxicillin ambroxol granules, etc.
Recently, according to the report of the marketing department, Nanchang Feihong Pharmaceutical Co., Ltd. signed the 17.5m3 walk-in drug stability inspection room of our company. In the early stage, both parties explained and confirmed the structure, design and operation of the equipment. After the whole communication, the other side recognized the plan we provided. Now, our company is doing some preparatory work to facilitate the installation of auxiliary equipment as soon as possible. The following, to do the walk-in inspection room to provide some information for customers;
Temperature range: 0 ~ 65 ℃
Temperature fluctuation: ≤± 0.5 ℃
Humidity range: 20-95% RH
Humidity fluctuation: ≤± 1% RH
Controller: temperature and humidity integrated touch screen controller
Refrigeration system: totally enclosed high temperature resistant compressor
Power supply: AC220V / 50Hz or 380V / 50Hz
The size of inner cavity and outer box shall be customized according to customer's requirements or field installation size;
The step-by-step drug stability inspection room is to investigate the law of drug changes with time under the influence of temperature and humidity, to provide scientific basis for the production, packaging, storage and transportation conditions of drugs, and to establish the validity period of drugs through tests, which is applicable to the test of influencing factors, accelerated test and long-term test of drugs; our company provides free installation and debugging, such as 3Q verification, operation training And long-term after-sales service.
Recently, according to the report of the marketing department, Nanchang Feihong Pharmaceutical Co., Ltd. signed the 17.5m3 walk-in drug stability inspection room of our company. In the early stage, both parties explained and confirmed the structure, design and operation of the equipment. After the whole communication, the other side recognized the plan we provided. Now, our company is doing some preparatory work to facilitate the installation of auxiliary equipment as soon as possible. The following, to do the walk-in inspection room to provide some information for customers;
Temperature range: 0 ~ 65 ℃
Temperature fluctuation: ≤± 0.5 ℃
Humidity range: 20-95% RH
Humidity fluctuation: ≤± 1% RH
Controller: temperature and humidity integrated touch screen controller
Refrigeration system: totally enclosed high temperature resistant compressor
Power supply: AC220V / 50Hz or 380V / 50Hz
The size of inner cavity and outer box shall be customized according to customer's requirements or field installation size;
The step-by-step drug stability inspection room is to investigate the law of drug changes with time under the influence of temperature and humidity, to provide scientific basis for the production, packaging, storage and transportation conditions of drugs, and to establish the validity period of drugs through tests, which is applicable to the test of influencing factors, accelerated test and long-term test of drugs; our company provides free installation and debugging, such as 3Q verification, operation training And long-term after-sales service.