What is the legal framework governing the export of drugs?

In New Hampshire, pharmaceutical laws govern the export of drugs. The laws require that those involved in the export of drugs must first obtain an export license. This license is given out by the Division of Health and Human Services and is necessary for any shipment of pharmaceuticals or medical devices entering or leaving the United States. The Division of Health and Human Services also oversees and monitors the certification and authorization of individuals and organizations to export drugs. In order to be approved for an export license, the drug must have all necessary certifications from the Food and Drug Administration (FDA). The Drug Enforcement Administration (DEA) also plays a role in the export of drugs. The DEA issues certain registration requirements to manufacturers and distributors of controlled substances. Manufacturers must be registered with the DEA in order to manufacture, distribute, or dispense drugs that are classified as controlled substances. All export transactions must also be reported to the DEA and require prior approval. It is important to note that the exporting country may also have additional requirements that must be met before a drug can be exported. Ultimately, it is the responsibility of the exporter and importer to ensure that all laws and regulations are followed. The FDA, DEA, and Division of Health and Human Services work together to ensure that these laws are adhered to and that the export of drugs is done in a safe and legal manner.

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What is the legal framework governing the export of drugs?

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