Documentation requirements for import of specified categories of products under NAC-Chemicals

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....y the documents to be verified by Customs officers for each category: • Checklist I: Cosmetics • Checklist II: Drugs, including active pharmaceutical ingredients (APIs) and finished formulations • Checklist III: Import of drugs: * (a) For personal use * (b) Small quantities of a new drug imported by a Government hospital or autonomous medical institution for the treatment of patients • Checklist IV: Import of drugs for examination, test or analysis • Checklist V: Medical devices, including in vitro diagnostic (IVD) kits/ devices • Checklist VI: Import of medical devices • Checklist VII: Import of raw materials or components used in t....

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....ecklist I: Cosmetics S.No. Particulars 1 *Self-Certified copy of Registration Certificate (RC) in Form COS-2 in case of fresh registration or Form COS-4A in case of subsequent registration issued by CDSCO 2 Self-certified copy of invoice. •  The invoice of the consignment shall mention the name of the cosmetics and match with the RC with respect to the Pack size (in case of finished product) 3 Self-certified copy of packing list. 4 Self-certified copy of the certificate of country of origin. 5 Items shall be labelled and match with RC w.r.t. a. Name of the cosmetics b. RC No. of the cosmetics and the name and address of the registration certificate holder for marketing ....

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.... S.No. Particulars 1 Self-Certified copy of Registration Certificate (RC) in Form 41 along with Import License (IL) in Form 10 2 Self-Certified copy of invoice *The invoice of the consignment shall mention the name of the item and match with RC/IL with respect to the Pack size (in case of finished product). 3 Self-certified copy of packing list. 4 Self-certified copy of the certificate of country of origin. 5 Self-certified copy of labels and markings on the consignment. The Drug Items (API, Finished product) should be labelled and match with RC and IL with respect to the following :- a. Name of the drug b. IL No. and the name and address of the Import license holder. c. The ....

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..../manufacturing license) 8 Undertaking by the importer that the consignment packaging is not damaged/broken/destroyed and the content of the drug/cosmetic has not deteriorated. Note: The residual shelf life calculated on the date of import should be more than 60 %. If the Residual shelf life is less than 60%, the consignment should be referred to the concerned CDSCO port office. Checklist III: Checklist for Import of Drugs a. for personal use or, b. Import of small quantities of the new drug by a Government Hospital or Autonomous Medical Institution for the treatment of patients. S.No. Particulars 1 Self-certified copy of Import permission granted in Form 12B or Form 11A/CT-25 2 Self-certified ....

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....ces (Including IVD's i.e., in vitro diagnostics kits/devices) S.No. Particulars 1 Self-certified copy of Import License in Form MD-15 issued by CDSCO. *In case of Class A (non-sterile and non-measuring) medical devices, the registration number. 2 Self-Certified copy of invoice, packing list, certificate of country of origin * The invoice of the consignment shall mention the name of the item and match with the Import License (MD-15) with respect to the Pack size (in case of finished product). 3 Self-certified copy of packing list. 4 Self-certified copy of the certificate of country of origin. 5 Self-certified copy of labels and markings on the consignment. The medical devices shall be labelled an....