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SFDA Guide to Good Manufacturing Practice for Medicinal Products

On August 28, the Saudi Food and Drug Authority updated its "Guide to Good Manufacturing Practice for Medicinal Products".

The new version 4.1, contains the updated information related to the Manufacture Of Biological Medicinal Substances And Products For Human Use.


The GMP guideline contains 9 Chapters such as Pharmaceutical quality system, Personnel, Premises and equipment etc, and has 20 annexures and an appendix detailing how to guide the Manufacture Of Biological Medicinal Substances And Products For Human Use.


Click this LINK to know more about SFDA's Guide to Good Manufacturing Practice for Medicinal Products.











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