The U.S. Food and Drug Administration (FDA) closely monitors dietary supplement manufacturing through inspections. When problems are found, the agency issues Form 483 observations, which list the ways a company has failed to meet current Good Manufac
Current Good Manufacturing Practices (cGMPs), found in 21 CFR Part 111, are often seen as rules to protect customers and product quality. But they also protect the people who make the products, you and your team. Whether you’re a line worker, supe
If you run or manage a dietary supplement facility, you're probably aware of FDA’s current Good Manufacturing Practices (cGMPs) under 21 CFR Part 111. You may have protocols for sanitation, batch records, supplier qualification, and equipment checks.
