How has the regulation of pharmaceuticals changed over the years?

Over the last century, the regulation of pharmaceuticals has changed significantly in North Carolina. Initially, drugs were regulated by state governments, allowing for them to vary from state to state. This left it up to individuals to decide if they wanted to purchase certain drugs or not. This form of regulation was often ineffective in protecting the safety and health of the public, as there were no standards for the production, distribution, or sale of drugs. In 1938, the federal government passed the Federal Food, Drug, and Cosmetic Act. This act was designed to protect consumers from unsafe or ineffective drugs, and it is still the cornerstone of the regulation of pharmaceuticals today. It required that drugs be proven safe before they could be marketed and sold, and it established the first rules to regulate pharmaceutical manufacturing. In recent years, the regulations have become more stringent. For example, the North Carolina Department of Health and Human Services now requires that pharmaceuticals must be approved by the US Food and Drug Administration to be sold in the state. The FDA also requires that manufacturers adhere to the Current Good Manufacturing Practices regulations, which has helped to ensure the safety of the public. In addition to these new regulations, there have also been changes to how pharmaceuticals are paid for and who is able to access them. For instance, North Carolina has recently passed legislation that requires insurance companies to offer coverage for certain medications. These changes have helped to ensure that consumers can access the treatment they need while also ensuring the safety and efficacy of the products.

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