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    <title>Government Takes Action for Complying with New Standards for Import of Bulk Drugs into EU</title>
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    <description>Exporters of Active Pharmaceutical Ingredients must obtain a written confirmation from a nominated national authority that the API and its manufacturing facility comply with EU GMP and are subject to equivalent GMP control and enforcement. The authority will require a prescribed application, document completeness checks, inspection where appropriate, and will communicate any non compliance to the EU. Satisfactory applications are processed within an administrative timetable and issued confirmations carry a defined multi year validity.</description>
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