
Pharmaceutical Regulatory Agencies
Pharmaceutical regulatory agencies are government organizations responsible for ensuring the safety, efficacy, and quality of medications before they are approved for public use. They review research and clinical trial data submitted by drug manufacturers, monitor side effects, and enforce regulations to protect public health. Notable examples include the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). By overseeing the drug approval process and continuing to monitor medications after they are on the market, these agencies help ensure that the medicines we use are safe and effective.