prescription drug approval

Prescription drug approval is a process where a regulatory agency, like the FDA, evaluates a new medication to ensure it is safe and effective for patients. Developers conduct rigorous testing through multiple phases, including laboratory research, animal studies, and human clinical trials. The agency reviews all data to assess potential risks and benefits. If the benefits outweigh the risks, the medication is approved for patient use. This process helps protect public health by ensuring medications meet strict quality standards before they are available in healthcare settings.