In July 2015, CFDA issued relevant documents, requiring manufacturers to have the ability and conditions for testing sterility, microbial limits and positive controls, and those who are engaged in work affecting product quality should undergo corresponding technical training and have relevant theoretical knowledge and practical knowledge. operational skills. According to the requirements of the “Good Manufacturing Practice for Drugs”, all personnel related to the quality of drug production should undergo training, and the content of the training should be adapted to the requirements of the post.
Post time: Jun-27-2020