Introduction|General Provisions|Facilities and Equipment|Manufacturing and Labeling|Laboratory Controls and Records|GMP Documentation
Good Manufacturing Practices (GMPs) keep consumers safe and companies in compliance with the law. The pharmaceutical manufacturing industry is governed by them through the Food & Drug Administration’s (FDA) Code of Federal Regulations (CFR) Title 21 Parts 210 & 211. This health and safety training course gives an overview of these regulations. . The FDA requires documentation of each stage in the manufacturing process, from receiving materials to distributing the finished product. Viewers learn GMP documentation must show compliance with GMPs that processes were controlled and consistent, and who was responsible. The documentation must also provide follow-up on the product after distribution. Watch this health and safety course to help ensure compliance with the CFR parts 210 & 211.