What is a primary purpose of FDA regulation of drugs?

The primary purpose of FDA regulation of drugs is to ensure the safety and efficacy of medications. The FDA establishes rigorous standards that drugs must meet before they can be approved for public use. This process includes preclinical testing, clinical trials, and a thorough review of the drug's ingredients, manufacturing processes, and labeling. By focusing on safety, the FDA aims to minimize risks to patients while ensuring that the medications provide the intended therapeutic benefits. This regulatory framework is crucial for protecting public health and maintaining trust in the pharmaceutical system.

In contrast, ensuring marketing success, regulating food products, and increasing consumer choice are not the main objectives of the FDA concerning drug regulation. While these aspects may be influenced by regulatory actions, they do not reflect the core mission of the FDA, which is primarily concerned with safeguarding health through the assessment of drugs for safety and effectiveness before they reach the market.