Since founded, Panlong Yunhai has always conscientiously implemented the Good Manufacture Practice (GMP) of medical products as well as applicable laws and regulations on food, health food, cosmetics and medical device production. In addition, we uphold the quality idea that “product quality depends on production instead of testing” and emphasize quality control in the process of production to try to eliminate hidden danger for quality problems. We continuously deepen GMP management, attach great importance to the optimization and innovation of hardware technology, improve software system management and put training and improving the employees’ quality and operating skills at the first place. We continuously improve the quality assurance system, gradually developing a quality control and assurance system with “zero defect” covering such sectors as product design, research, development, purchase of raw materials, acceptance examination, in-process control, packaging and warehousing, sales and user feedback and adverse reaction report. We implement standardized, routinized and systematic production quality control. 


  1. Quality assurance system construction. The company has established the organization structure meeting the requirements for product manufacturing and quality control with six departments and one office set. Each department has specific functions and duties and coordinates each other in work to realize sound management and smooth communication. The company is staffed with quality control personnel fit for the products covering QC and QA systems. Staffing may ensure to complete necessary work of product quality testing and production process control. At the same time, a whole set of production quality control file system is established to realize quality control in each part of the production, connect the whole production process link by link, make each step controllable and realize orderly operation. 


2. Continuously improve management software system. With more than twenty years’ development, the software system of the company has also been added and improved continuously to make the production quality control activities based on rules and to realize standardized, routinized and systematic quality control. 


3. Enhance management of all the employees’ sense of quality. The company breaks down the responsibility for quality to each department, workshop, shift and operating post. Reverse-direction supervision and evaluation of product quality is carried out in each part of the whole production process between working procedures to enhance the employees’ sense of quality and communicate to each employee the idea that product quality safety is the responsibility of everyone. 


4. The company enhances process and quality control and makes checks at all levels for materials, production process, semi-finished products and finished products. The company has established a quality assurance system of whole-process monitoring covering such sectors as purchase of raw and auxiliary materials, acceptance examination, in-process control, packaging and warehousing, sales, user feedback and adverse reaction monitoring report so as to realize quality control in each part of the production, connect the whole production process link by link, make each step controllable and realize orderly operation.


5. Rigorous management of drug traceability system. The company has established the drug traceability system platform to realize uninterrupted traceability of product quality and ensure drug quality traceability.