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  1. www.ecfr.gov › current › title-2121 CFR Part 211 -- Current Good Manufacturing Practice for...

    Link to an amendment published at 89 FR 51769, June 18, 2024. ( a) The regulations in this part contain the minimum current good manufacturing practice for preparation of drug products (excluding positron emission tomography drugs) for administration to humans or animals.

  2. www.accessdata.fda.gov › scripts › cdrhCFR - Code of Federal Regulations Title 21 - Food and Drug...

    Mar 22, 2024 · TITLE 21--FOOD AND DRUGS. CHAPTER I--FOOD AND DRUG ADMINISTRATION. DEPARTMENT OF HEALTH AND HUMAN SERVICES. SUBCHAPTER C - DRUGS: GENERAL. Subpart A - General Provisions. § 211.1 - Scope. §...

  3. www.ecfr.gov › current › title-21eCFR :: 21 CFR Part 211 -- Current Good Manufacturing Practice...

    View Title 21 on govinfo.gov; View the PDF for 21 CFR Part 211; These links go to the official, published CFR, which is updated annually. As a result, it may not include the most recent changes applied to the CFR. Learn more.

  4. www.accessdata.fda.gov › scripts › cdrhCFR - Code of Federal Regulations Title 21 - Food and Drug...

    Mar 22, 2024 · TITLE 21--FOOD AND DRUGS. CHAPTER I--FOOD AND DRUG ADMINISTRATION. DEPARTMENT OF HEALTH AND HUMAN SERVICES. SUBCHAPTER C - DRUGS: GENERAL. Subpart D - Equipment. Sec. 211.63 Equipment design,...

  5. ecfr.io › Title-21 › Part-21121 CFR §211 Current Good Manufacturing Practice For Finished ...

    part 211 - current good manufacturing practice for finished pharmaceuticals . authority: 21 u.s.c. 321, 351, 352, 355, 360b, 371, 374; 42 u.s.c. 216, 262, 263a, 264. Source: 43 FR 45077, Sept. 29, 1978, unless otherwise noted.

  6. www.accessdata.fda.gov › scripts › cdrhCFR - Code of Federal Regulations Title 21 - Food and Drug...

    Mar 22, 2024 · TITLE 21--FOOD AND DRUGS. CHAPTER I--FOOD AND DRUG ADMINISTRATION. DEPARTMENT OF HEALTH AND HUMAN SERVICES. SUBCHAPTER C - DRUGS: GENERAL. Subpart J - Records and Reports. Sec. 211.180 General...

  7. www.fda.gov › drugs › pharmaceutical-quality-resourcesCurrent Good Manufacturing Practice (CGMP) Regulations | FDA

    Dec 29, 2023 · Code of Federal Regulations (CFR) FDA's portion of the CFR is in Title 21, which interprets the Federal Food, Drug and Cosmetic Act and related statutes, including the Public Health Service Act...

  8. www.law.cornell.edu › cfr › text21 CFR Part 211 - LII / Legal Information Institute

    LII. Electronic Code of Federal Regulations (e-CFR) Title 21—Food and Drugs. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES. SUBCHAPTER C—DRUGS: GENERAL. PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS.

  9. www.accessdata.fda.gov › scripts › cdrhCFR - Code of Federal Regulations Title 21 - Food and Drug...

    Mar 22, 2024 · PART 211. CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS. Subpart A - General Provisions. Sec. 211.1 Scope. (a) The regulations in this part contain the minimum current good...

  10. www.accessdata.fda.gov › scripts › cdrhCFR - Code of Federal Regulations Title 21 - Food and Drug...

    Mar 22, 2024 · PART 211 -- CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS. Subpart C - Buildings and Facilities