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兽药GMP是《兽药生产质量管理规范》的简称,是指在兽药生产全过程中,用科学合理、规范化的条件和方法来保证生产优良兽药的整套科学管理体系。兽药GMP实施过程中可以分为3部分,即硬件购置、软件编写、人员培训。对于这3个关键项目,许多企业都会出现一些认识上的错误,认为软件编写是重要的,对于硬件购置,只要有钱就能办好,而对于人员培训,随便培训一下就行。重视软件编写,但不能轻视硬件购置,更不能忽略人员的培训。许多企业不能顺利通过GMP验收,不是硬件设置的不够好,也不是软件编写的不够完善,而是人员素质不过关。因此,在兽药GMP改造中,要重视人员的培训。
Veterinary drug GMP is short for “Code of Quality Control for Veterinary Drug Production” and refers to the whole set of scientific management system of ensuring the production of veterinary drugs with scientific, reasonable and standardized conditions and methods in the whole process of veterinary drug production. Veterinary drug GMP implementation process can be divided into three parts, namely, hardware acquisition, software preparation, personnel training. For these three key projects, many companies will make some mistakes in understanding, that the preparation of the software is important for hardware acquisition, as long as the money can be good, but for staff training, just train on the line. Pay attention to the preparation of software, but can not underestimate the hardware purchase, but can not ignore the training of personnel. Many companies can not pass the GMP acceptance, not hardware is not good enough, nor is the software is not perfect, but the quality of personnel but pass. Therefore, in the reform of veterinary drugs GMP, we should pay attention to personnel training.