What are the regulations regarding the distribution of pharmaceuticals?

In North Carolina, the distribution of pharmaceuticals is regulated by state and federal laws. These regulations are in place to protect the safety and quality of pharmaceuticals and to ensure their proper distribution. In order to distribute pharmaceuticals in North Carolina, companies must first obtain a wholesaler permit from the North Carolina Board of Pharmacy. This permit allows them to sell prescription and over-the-counter drugs to retailers, hospitals, and other wholesale drug distributors. In order for a company to obtain a wholesaler permit, the company must pass an inspection, pay an annual fee, and maintain the necessary records. In addition to the wholesaler permit, companies must also maintain a Drug Distributor Registration. This registration requires companies to keep records of all their transactions, notify the Board of Pharmacy of any changes in their operations, and submit an annual statement of the drugs they distribute in North Carolina. Finally, companies must abide by federal regulations when distributing pharmaceuticals. These regulations include the Federal Food, Drug, and Cosmetic Act, which provides standards for ensuring the safety, quality, and purity of pharmaceuticals. In addition, companies must comply with the Drug Supply Chain Security Act, which regulates how pharmaceuticals are traced from the manufacturer (or repackager) to the patient. By following these regulations, companies can help ensure that the pharmaceuticals they distribute are safe and effective. This helps protect the health of North Carolinians and allows them to access the quality medications they need.

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What are the regulations regarding the distribution of pharmaceuticals?

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