21 CFR Parts 210-211
21 CFR Parts 210-211 contain the minimum Current Good Manufacturing Practice (cGMP) for methods to be used in - and the facilities or controls to be used for - the manufacture, processing, packing, or holding of drug products to ensure that such drugs meet regulatory requirements of the act as to safety, identity, strength, quality, and purity characteristics that it implies or is represented to possess.
This is only an overview/extract of the standard. Users should not rely on its accuracy, but should refer to the complete standard of the appropriate revision.
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