What is the legal framework governing the export of drugs?

In Kansas, the legal framework governing the export of drugs is governed by federal and state laws. The Food and Drug Administration (FDA) is responsible for monitoring and regulating the export of drugs, both pharmaceutical and non-pharmaceutical drugs, through its Export Administration Regulations (EAR). The EAR states that any drug intended for export must be approved by the FDA. It also requires manufacturers and exporters to provide licenses to export drugs to other countries. The FDA also inspects pharmaceutical facilities prior to any drug being exported and those facilities must comply with the GMP (Good Manufacturing Practices) to ensure the safety and quality of the drugs. In addition, any export of a pharmaceutical drug must follow the Kansas Pharmacy Law which outlines the requirements for importing and exporting drugs within the state. The law requires all pharmaceutical products to be tested and approved by the Kansas Board of Pharmacy, prior to sale and distribution. The Kansas Department of Agriculture (KDA) also has the authority to regulate exports of drugs, as well as inspect plants and facilities for compliance. All exporters, manufacturers, and distributors in Kansas must register with the KDA in order to export drugs to foreign countries. Overall, the legal framework in Kansas is designed to ensure the safety of drugs that are being exported and to protect consumers from harmful products.

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