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发表于 2018-5-17 21:27:21
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本帖最后由 beiwei5du 于 2018-5-17 21:28 编辑
直接上FDA原文吧。
那篇文章存在多处基础性的错误,不知道是什么时候写的。
The CGMP requirements were established to be flexible in order to allow each manufacturer to decide individually how to best implement the necessary controls by using scientifically sound design, processing methods, and testing procedures. The flexibility in these regulations allows companies to use modern technologies and innovative approaches to achieve higher quality through continual improvement. Accordingly, the "C" in CGMP stands for "current," requiring companies to use technologies and systems that are up-to-date in order to comply with the regulations. Systems and equipment that may have been "top-of-the-line" to prevent contamination, mix-ups, and errors 10 or 20 years ago may be less than adequate by today's standards
Facts About the Current Good Manufacturing Practices (CGMPs)
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