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Foreign manufacturing sites where FDA inspections are concentrated More than 62% of FDA drug quality inspections in FY 2024 targeted foreign manufacturing sites, reflecting the increasingly global footprint of the pharmaceutical supply chain. Combined with the Green List initiative and a growing list of import alerts covering non-compliant foreign facilities, the picture is one of intensifying supply chain enforcement. For organizations that manufacture or source APIs overseas or that rely on contract manufacturers who do regulatory exposure is meaningfully higher than for purely domestic operations, and due diligence on supplier GMP status has become a frontline compliance activity rather than a periodic check

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