What is the legal framework governing the sale of prescription drugs?

Prescription drug sales are governed by a legal framework in Illinois to ensure they are safe, effective, and accessible. This framework includes laws, administrative rules, and regulations. The Illinois Pharmacy Practice Act (PPA) is the main piece of legislation governing the sale of prescription drugs. It defines the scope of practice for pharmacists and other health care professionals licensed to dispense drugs. The PPA also provides guidelines for the safe and effective distribution of prescription drugs, as well as rules for labeling, packaging, and storage. Pharmacies must also adhere to strict standards of professional conduct set by the Department of Financial and Professional Regulation (IDFPR). The Drug and Cosmetic Act (DCA) is another law relevant to the sale of prescription drugs. This Act ensures that all prescription and over-the-counter drugs sold in Illinois meet certain standards for safety and efficacy. The DCA also sets forth rules for labeling, packaging, and advertising. The Food and Drug Administration (FDA) also has a role in governing prescription drug sales. The FDA is responsible for ensuring that drugs are safe and effective before they are approved for sale. The FDA also inspects manufacturing facilities and conducts investigations to make sure drug companies comply with the law. Finally, it is important to note that pharmacies must also abide by the terms of their contracts with payers. These contracts may include restrictions on which drugs pharmacies can dispense, as well as rules for handling and billing for prescription drugs. All of these laws, regulations, and guidelines act together to create a legal framework regulating the sale of prescription drugs. This framework serves to protect the public from potentially dangerous drugs and ensure that all prescription drugs are safe, effective, and accessible.

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What is the legal framework governing the sale of prescription drugs?

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