Drug Regulatory Authorities

Drug Regulatory Authorities are government agencies responsible for ensuring the safety, efficacy, and quality of medicines and healthcare products. They evaluate new drugs before approval, monitor their use post-market, and enforce standards to protect public health. These authorities also oversee manufacturing practices and handle drug recalls if necessary. Their role helps prevent unsafe or ineffective medications from reaching consumers and ensures that healthcare products meet established safety and quality standards. Examples include the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA).