How has the regulation of pharmaceuticals changed over time?

Over time, the regulation of pharmaceuticals has evolved significantly in Alabama. In the mid-1800s, the state implemented the pharmacy act of 1856, which created the state’s first board of pharmacy to license and regulate pharmacists. This board was created in response to the growing number of untrained pharmacists, who were not qualified to dispense medications safely and effectively. In the late 1800s, the State Board of Pharmacy was given the power to regulate the distribution and sale of narcotics and poisons in the state. This board was eventually disbanded, and its responsibilities were passed onto the Alabama Board of Health. In the early 1900s, Alabama began regulating drug manufacturing and wholesaling. The state created a Drug Control section in the Department of Health to monitor and inspect licensed drug wholesalers and manufacturers in the state. This section was eventually dissolved and the powers to regulate drugs were given to the Alabama Division of Professional and Occupational Regulation. Today, the Alabama Department of Public Health regulates the sale and sale of drugs, medical devices, and other pharmaceuticals in the state. Their efforts are aimed at ensuring that medications are dispensed safely and accurately to protect the public from harm. In addition, the Federal Drug Administration (FDA) also regulates the production and labeling of drugs in the state to ensure that they are safe and effective for use.

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