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Compact Regs Parts 210 and 211. Content: Book Cover; Title; Copyright; PART 210-CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL; PART 211--CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS; KEYWORD INDEX TO 21 CFR PARTS 210 AND 211. Abstract: Compact Regs Parts 210 and 211
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The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments.
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