Who oversees the compliance with the Prescription Drug Marketing Act 1987?

The compliance with the Prescription Drug Marketing Act of 1987 is overseen by the Food and Drug Administration (FDA). This act was established to ensure the integrity of the pharmaceutical supply chain and prevent counterfeit drugs from entering the marketplace. The FDA is responsible for regulating the marketing and distribution of prescription drugs, ensuring that manufacturers and wholesalers adhere to safe and legal practices.

Additionally, the FDA has the authority to enforce the provisions of the act, which include regulating the samples of prescription drugs that can be distributed and establishing guidelines for the wholesale distribution of prescription medications. This oversight is crucial for maintaining public health and safety as it helps to guarantee that patients receive the medications they require from legitimate sources.

The other entities mentioned, such as the Federal Bureau of Investigation and the Department of Health and Human Services, have other roles related to public health and law enforcement but do not specifically manage compliance with the Prescription Drug Marketing Act. The State Board of Pharmacy primarily focuses on state-level regulation and licensing of pharmacists and pharmacies rather than federal compliance issues.