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《药品生产管理规范》(简称药品GMP)是药品全面质量管理的重要组成部分,是在药品生产的全过程中,把发生差错、混药及各种污染的可能性降至最低程度的必要条件和最可靠的
The “Code of Pharmaceutical Production Management” (referred to as the drug GMP) is an important part of the total quality management of medicines and is the necessary condition for minimizing the possibility of errors, drug mixing and various kinds of pollution in the whole process of drug production And the most reliable