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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21—Food and Drugs
  4. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER B—FOOD FOR HUMAN CONSUMPTION
  6. PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
  7. Subpart J—Production and Process Control System: Requirements for Laboratory Operations

21 CFR Part 111 - Subpart J - Production and Process Control System: Requirements for Laboratory Operations

  • CFR
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  1. § 111.303 What are the requirements under this subpart J for written procedures?
  2. § 111.310 What are the requirements for the laboratory facilities that you use?
  3. § 111.315 What are the requirements for laboratory control processes?
  4. § 111.320 What requirements apply to laboratory methods for testing and examination?
  5. § 111.325 Under this subpart J, what records must you make and keep?

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