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        Congratulations on Tongtai bio's GMP retest

        On August 29-30, 2020, at the invitation of Jiangsu Provincial Department of agriculture and rural areas, the GMP expert group of the Ministry of agriculture and rural areas conducted the GMP re acceptance of Changzhou Tongtai Biopharmaceutical Technology Co., Ltd.
        Accompanied by the leaders of the Veterinary Bureau of the provincial agriculture and rural department, the inspection team conducted a comprehensive inspection on the operation and implementation of GMP for veterinary drugs in our company in the past five years. It was found that Tongtai biological had a sound organization, clear job responsibilities, qualified personnel structure, quality and training, and production management and quality management met the requirements of GMP for veterinary drugs. Upon the decision of the inspection team, it was unanimously agreed to recommend the production lines of cytotoxic inactivated vaccine and embryotoxic inactivated vaccine of Changzhou Tongtai Biopharmaceutical Technology Co., Ltd., both of which are GMP qualified production lines for veterinary drugs.
        Signing ceremony of GMP acceptance
        The successful passing of the veterinary drug GMP re inspection is the recognition of the company's early conscientious implementation of the veterinary drug GMP specification. The company will take the re inspection as a new starting point, make persistent efforts, and thoroughly implement the quality concept and essence of the new version of veterinary drug GMP into the production and quality system, so as to provide a solid foundation and guarantee for the production of higher quality products.
         
         

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