Checklists for mandatory compliance for Cosmetics/Drugs/Medical Devices to be verified by the Customs officer before granting out-of-charge in case of PGA facilitated Bills of Entry
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Pre-clearance compliance for regulated imports requires verification of licences, labels, shelf life, quality certificates, and importer undertakings.
Customs out-of-charge clearance for PGA-facilitated cosmetics, drugs and medical-device imports requires verification of category-specific regulatory records before clearance. Required records include applicable registration, import or manufacturing licences and permissions, invoices, packing lists, country-of-origin certificates, compliant labels, batch quality certificates, storage-premises evidence and importer undertakings. Cosmetics, drugs and shelf-life-sensitive medical devices must meet prescribed labelling and residual shelf-life conditions. Drug and device permissions must correspond with the imported product and quantity. Discrepancies, doubts, deficient shelf life and specified new-product imports require referral to the relevant port office.