Importing cosmetics, drugs or medical devices: Customs to check CDSCO documents before out-of-charge — upload them on e-SANCHIT
Circular 40/2026-Customs circulates seven CDSCO checklists of licences, permissions and registration certificates that the Customs officer is to verify before releasing such imports, while their integration under SWIFT 2.0 is in process.
Key facts
- Who it affects
- Importers of cosmetics, drugs and medical devices
- What it is
- Action needed
- Section
- Customs
- Published
- 3 September 2026
In 30 seconds
- Seven checklists: cosmetics; drugs (API, finished formulation); drugs for personal use or by a Government hospital; drugs for test or analysis; medical devices including IVDs; import of medical devices; raw materials and components for medical devices.
- The documents are those required under the Drugs and Cosmetics Act, 1940 and its Rules.
- Importers are asked to upload the required documents on e-SANCHIT for faster clearance.
हिंदी में सार
कॉस्मेटिक्स, दवाओं और मेडिकल डिवाइस के आयात पर Customs अधिकारी out-of-charge देने से पहले CDSCO के दस्तावेज़ जाँचेगा। CBIC ने Circular 40/2026 में सात checklist जारी की हैं। आयातक ज़रूरी दस्तावेज़ e-SANCHIT पर अपलोड करें ताकि क्लियरेंस जल्दी हो।
What Customs has been told
Cosmetics, drugs and medical devices need licences, permissions and registration certificates under the Drugs and Cosmetics Act, 1940 and the Rules made under it. Integration of these documents under SWIFT 2.0 is in process. Until then, CBIC has asked field formations to exercise due diligence and check the documents at the time of out-of-charge for Bills of Entry facilitated by the partner Government agency.
The seven checklists
- Cosmetics
- Drugs — Active Pharmaceutical Ingredient and finished formulation
- Import of drugs for personal use, and of small quantities of a new drug by a Government hospital or autonomous medical institution for treatment of patients
- Import of drugs for examination, test or analysis
- Medical devices, including in-vitro diagnostic kits and devices
- Import of medical devices
- Import of raw materials and components used for manufacture of medical devices
For cosmetics, the checklist starts with a self-certified copy of the Registration Certificate issued by CDSCO — Form COS-2 for a fresh registration or Form COS-4A for a subsequent one — and a self-certified copy of the invoice.
What importers should do
- Read the checklist for your product category in Annexure-A of the circular.
- Upload each listed document on e-SANCHIT with the Bill of Entry.
Published 3 September 2026. Updated 7 October 2026. This report is for general information and is not professional advice. Read the source document before acting on it.