cGMP stands for Current Good Manufacturing Practices, which are regulations enforced by the FDA to ensure that pharmaceutical companies adhere to strict standards throughout their processes, from raw material sourcing to the release of medicinal products. The regulations make sure that a product is safe for use, and that it has the ingredients and strength it claims to have. cGMP provides a system of processes, controls, and documentation to ensure the safety, quality, and efficacy of pharmaceutical products. Adherence to the cGMP regulations assures the identity, strength, quality, and purity of drug products by requiring that manufacturers of medications adequately control manufacturing operations. The guidelines are designed to prevent errors and contamination during all stages of drug manufacturing, from raw materials to finished products. The importance of cGMP manufacturing lies in protecting patients in an industry where the stakes are high.