What is the general purpose of the Federal government in healthcare regulation?

The general purpose of the Federal government in healthcare regulation focuses primarily on ensuring medication safety and efficacy. This includes the responsibility of agencies like the Food and Drug Administration (FDA) to oversee the approval process for new medications, monitor the safety of drugs in the market, and regulate labeling and advertising practices. By maintaining strict standards in drug development and distribution, the Federal government seeks to protect public health and ensure that only safe and effective pharmaceuticals are available to consumers.

While state-level grants, funding local hospitals, and establishing healthcare facilities can play important roles in the healthcare system, these activities are often driven by state and local governments rather than being a direct focus of federal regulation. The federal government's regulatory framework, primarily through agencies such as the FDA and the Centers for Medicare & Medicaid Services (CMS), centers on maintaining the integrity of healthcare products and services, emphasizing the safety and effectiveness of medications.