regulatory approval processes

Regulatory approval processes are the formal reviews by government agencies to ensure that new medical products, like drugs or devices, are safe and effective for public use. Developers submit detailed evidence from testing and clinical trials. Regulators then assess this data, evaluating potential risks and benefits, and ensuring manufacturing quality. If the product meets all standards, the agency grants approval, allowing it to be marketed and used by patients. This process helps protect public health by ensuring that only thoroughly evaluated, reliable products are available.