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Product Quality of Anhui Jiren Pharmaceutical Co., Ltd.
(1) Medicinal materials are the key to drug quality. High-quality green Chinese herbal medicine is the first guarantee for the quality of modern Chinese medicine. Jiren Pharmaceutical established a green standardized planting (GAP) base in Bozhou. Based on Anhui College of Traditional Chinese Medicine, the base actively promotes the achievements of the company's "Research on the Industrialization of Standardized Planting and Processing of Green Authentic Chinese Herbal Medicines". Jiren Pharmaceutical requires all Chinese herbal medicines and raw and auxiliary materials to be of high quality, and takes suppliers as the first workshop, and sets up special personnel to evaluate the qualifications of all suppliers; Implement dynamic management of suppliers, and eliminate them immediately if quality problems are found in the supplied goods; Suppliers are also re-evaluated regularly, and those that do not meet the requirements should be eliminated.
(2) Leading technology is the second guarantee for the quality of modern Chinese medicine in Jiren Pharmaceutical. Enterprises apply the most advanced technology and equipment combination in China to the production process of traditional Chinese medicine, and widely apply computer integrated control technology, and the production technology has reached the international advanced level.
(3) Advanced quality inspection and analysis instruments, high-quality professional quality management team and advanced technologies such as fingerprints are the third guarantee for the quality of modern Chinese medicine in Jiren Pharmaceutical. Jiren Pharmaceutical has established a strict quality control system and formulated internal control standards and inspection operation procedures for raw materials, semi-finished products and finished products. Formulate sampling and sample retention observation system; Formulate management measures for inspection equipment, instruments, reagents, test solutions, standards and titrant solutions, determine the use of materials and intermediate products, review relevant records before drug release, review the handling procedures of unqualified products, be responsible for sampling, inspection and sample retention of materials, semi-finished products and finished products, issue inspection reports, monitor the number of dust particles and microorganisms in clean areas, evaluate the quality stability of raw materials, semi-finished products and finished products, and determine the storage period and quality of materials. Formulate the responsibilities of quality management and inspection personnel to ensure that unqualified raw materials are not put into production, unqualified semi-finished products do not flow into the next working procedure, and unqualified finished products do not leave the factory.
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