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 H - Production and Process Control System: Requirements for the Master Manufacturing Record |
§ 111.205 - What is the requirement to establish a master manufacturing record? |
§ 111.210 - What must the master manufacturing record include? |