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2003年是我国监督实施药品GMP至关重要的一年。一方面是到最后时限的时间已经不多了,另一方面是按照《药品法》的规定,开始按药品类别剂型实施国家局和省级局两级认证,面对着繁重的工作任务和新的形势,必须坚定信心扎实工作,切实按照“统一标准、规范监督、保证质量、促进发展”的原则,确保按期实现药品GM[P的规划目标,保证人民用药安全有效。
2003 is the crucial year for our country to supervise the implementation of pharmaceutical GMP. On the one hand, the deadline has not expired. On the other hand, in accordance with the provisions of the Drug Law, it has started to implement the two-level certification of the State Bureau and the provincial bureau according to the type of pharmaceutical products. In the face of heavy workload and new tasks We must firmly believe in our efforts to work in a down-to-earth manner and earnestly follow the principle of “unifying standards, standardizing supervision, ensuring quality, and promoting development” so as to ensure that the goals of GM [P] in pharmaceuticals are achieved on schedule and that people’s medicines are safe and effective.