Food and Drug Administration

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Compact Regs Part 26 : CFR 21 Part 26 Mutual Recognition: US and the European Community

by Food and Drug Administration First published in 2001 — 4 editions

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Compact Regs Part 58: CFR 21 Part 58 Good Laboratory Practice for Non-Clinical Laboratory Studies

by Food and Drug Administration First published in 2002 — 4 editions

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Compact Regs Parts 50, 54, 56, And 312: CFR 21 Parts 50, 56, and 312 Good Clinical Practices

by Food and Drug Administration First published in 2002 — 4 editions

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Compact Regs Part 11 : CFR 21 Part 11 Electronic Records: Electronic Signatures

by Food and Drug Administration First published in 2002 — 3 editions

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Compact Regs CFR 21: Part 820, Quality System Regulation (10-pack)

by Food and Drug Administration First published in 2001 — 2 editions

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Compact Regs CFR 21 Part 11: Part 11, Electronic Records; Electronic Signatures (10-pack)

by Food and Drug Administration First published in 2003 — 1 edition

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Compact Regs CFR 21 Part 26: Part 26, Mutual Recognition: US and the European Community (10-pack)

by Food and Drug Administration First published in 2002 — 1 edition

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Compact Regs CFR 21 Part 58: Part 58, Good Laboratory Practice for Nonclinical Laboratory Studies (10-pack)

by Food and Drug Administration First published in 2003 — 1 edition

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Compact Regs CFR 21 Part 606: Part 606, Current Good Manufacturing Practice for Blood and Blood Components (10-pack)

by Food and Drug Administration First published in 2002 — 1 edition

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Compact Regs CFR 21 Part 820 April 2002 Revision: Part 820 April 2002 Revision, Quality System Regulation (10-pack)

by Food and Drug Administration First published in 2003 — 1 edition

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Compact Regs CFR 21 Parts 110 and 111: Parts 110 and 111, cGMP in Manufacturing, Packaging, or Holding Human Food, cGMP for Dietary Supplements

by Food and Drug Administration First published in 2002 — 1 edition

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Compact Regs CFR 21 Parts 201, 202, and 203: Parts 201, 202, and 203, Prescription Drug Labeling, Advertising and Marketing (10-pack)

by Food and Drug Administration First published in 2002 — 1 edition

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Compact Regs CFR 21 Parts 210 and 211: Parts 210 and 211, Pharmaceutical and Bulk Chemical GMPs (10-pack)

by Food and Drug Administration First published in 2003 — 1 edition

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Compact Regs CFR 21 Parts 50, 56, and 312: Parts 50, 56, and 312, Good Clinical Practices (GCP) (10-pack)

by Food and Drug Administration First published in 2003 — 1 edition

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Compact Regs CFR 21 Parts 807, 812, & 814: Parts 807, 812, & 814, Medical Device Approval (10-pack)

by Food and Drug Administration First published in 2002 — 1 edition

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FDA Investigations Operations Manual

by Food and Drug Administration First published in 2003 — 1 edition
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Guideline: Validation of Cleaning Processes (Report)

by Food and Drug Administration First published in 1993 — 1 edition

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High Purity Water Systems (Report)

by Food and Drug Administration First published in 1993 — 1 edition

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Interpharm Master Keyword Guide to 21 CFR Regulations of the U.S. Food and Drug Administration (Fda-21 Cfr)

by Food and Drug Administration First published in 2001 — 1 edition

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Food Code '99: 1999 Recommendations of the United States Public Health Service, Food and Drug Administration

by United States. Department of Health and ..., Public Health Service, and Food and Drug Administration First published in 1999 — 1 edition

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OLID: OL3255797A

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Created April 30, 2008
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April 30, 2008

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Food and Drug Administration

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