What are the legal requirements for the supply of drugs?

In Oregon, the legal requirements for the supply of drugs are outlined in the state’s pharmacy law. This law includes rules and regulations for the manufacturing, compounding, packaging, labeling, and distribution of pharmaceuticals. Any pharmacy or drug wholesaler in Oregon must obtain a license from the Oregon State Board of Pharmacy, and any drug manufacturer must obtain an Oregon Certificate of Free Sale to operate legally. The Oregon Pharmacy Law also outlines how drugs must be labeled and stored. Drugs must be labeled in English, and at least one other language, and must include information such as the name of the product, manufacturer, date of manufacture, dosage form, instructions for use, side effects, and expiration date. Pharmacies and drug retailers must also store drugs in a secure or locked area, and must have a system in place to ensure that no unauthorized person can access the drugs. In addition, pharmacies and drug manufacturers must also adhere to FDA guidelines with regards to the safety of the drugs they produce and dispense. Drugs must be tested for quality and safety before being distributed, and must meet specific standards and protocols. The FDA also requires drug manufacturers to report any adverse side effects associated with the drugs they produce. Any violations of Oregon Pharmacy Law or FDA guidelines can result in the suspension or revocation of the pharmacy or drug manufacturer’s license.

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What are the legal requirements for the supply of drugs?

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