21 CFR Part 210 (Current Good Manufacturing Practice in Manufacturing Processing, Packing, or Holding of Drugs)

21 CFR Part 210 establishes regulations for the proper manufacturing, processing, packing, and holding of drugs to ensure safety, quality, and effectiveness. It requires pharmaceutical companies to follow strict standards for cleanliness, equipment, personnel training, and documentation. The goal is to prevent contamination, mix-ups, and errors throughout the drug production process. Regular audits and quality checks are mandated to maintain high standards. Overall, it helps ensure that medicines are consistently safe for patients by enforcing best practices in pharmaceutical manufacturing.