pharmaceutical regulation

Pharmaceutical regulation involves the oversight of the development, approval, and marketing of medications to ensure they are safe, effective, and of high quality. National and international agencies, like the U.S. Food and Drug Administration (FDA), assess new drugs through rigorous scientific research and testing before they can be sold to the public. These regulations aim to protect public health by ensuring that medications meet strict safety standards and that consumers are adequately informed about their benefits and risks. This process helps maintain trust in the healthcare system and promotes innovation in drug development.