Code of Federal Regulations (Last Updated: July 5, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter B - Food for Human Consumption |
Part 111 - Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements |
Subpart J - Production and Process Control System: Requirements for Laboratory Operations |
§ 111.303 - What are the requirements under this subpart J for written procedures? |
§ 111.310 - What are the requirements for the laboratory facilities that you use? |
§ 111.315 - What are the requirements for laboratory control processes? |
§ 111.320 - What requirements apply to laboratory methods for testing and examination? |
§ 111.325 - Under this subpart J, what records must you make and keep? |