What is FDA and GMP procedure?

The FDA, or Food and Drug Administration, is a U.S. government agency responsible for regulating food, pharmaceuticals, medical devices, and other health-related products to ensure their safety and efficacy. GMP, or Good Manufacturing Practice, refers to a set of guidelines and regulations enforced by the FDA to ensure that products are consistently produced and controlled according to quality standards. These procedures cover all aspects of production, from raw materials to facility hygiene, ensuring that products meet safety and quality requirements before they reach consumers. Compliance with FDA regulations and GMP is essential for manufacturers to ensure the integrity and reliability of their products.