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Title 21 —Food and Drugs; Chapter I —Food and Drug Administration, Department of Health and Human Services; Subchapter C —Drugs: General; Part 210 —Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General § 210.2
PART 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL Authority: 21 U.S.C. 321, 351, 352, 355, 360b, 371, 374; 42 U.S.C. 216, 262, 263a, 264. Source: 43 FR 45076, Sept. 29, 1978, unless otherwise noted.
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 210—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL.
Pt. 210. PART 210—CURRENT GOOD MAN-UFACTURING PRACTICE IN MAN-UFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL. Sec. 210.1 Status of current good manufacturing practice regulations. 210.2 Applicability of current good manu-facturing practice regulations. 210.3 Definitions.
Nov 16, 2022 · The CGMP regulations (21 CFR parts 210 and 211) for finished pharmaceutical manufacturing do not specifically address the requirement to conduct, or to keep records of, internal quality...
Dec 22, 2023 · [CITE: 21CFR210] TITLE 21--FOOD AND DRUGS. CHAPTER I--FOOD AND DRUG ADMINISTRATION. DEPARTMENT OF HEALTH AND HUMAN SERVICES. SUBCHAPTER C - DRUGS: GENERAL. Sec. 210.1 Status of current good...
Mar 12, 2004 · regulations (parts 210 and 211 and the 1978 Preamble to the CGMP regulations. 2) and various ... comprehensive quality systems can help manufacturers achieve compliance with 21 CFR parts . 4
