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Regulations last checked for updates: May 14, 2025

Title 21 - Food and Drugs last revised: May 12, 2025
All TitlesTitle 21Chapter IPart 117 - PART 117—CURRENT GOOD MANUFACTURING PRACTICE, HAZARD ANALYSIS, AND RISK-BASED PREVENTIVE CONTROLS FOR HUMAN FOOD
  • Subpart A [§ 117.1 - § 117.9] - Subpart A—General Provisions
  • Subpart B [§ 117.10 - § 117.110] - Subpart B—Current Good Manufacturing Practice
  • Subpart C [§ 117.126 - § 117.190] - Subpart C—Hazard Analysis and Risk-Based Preventive Controls
  • Subpart D [§ 117.201 - § 117.206] - Subpart D—Modified Requirements
  • Subpart E [§ 117.251 - § 117.287] - Subpart E—Withdrawal of a Qualified Facility Exemption
  • Subpart F [§ 117.301 - § 117.335] - Subpart F—Requirements Applying to Records That Must Be Established and Maintained
  • Subpart G [§ 117.405 - § 117.475] - Subpart G—Supply-Chain Program
authority: 21 U.S.C. 331,342,343,350d,350g,350g note,371,374; 42 U.S.C. 243,264,271
source: 80 FR 56145, Sept. 17, 2015, unless otherwise noted.
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