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Onboarding of CDSCO, WCCB, Textile Committee and MeitY on SWIFT 2.0 as Single Touch Point for Trade.

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प्रधानआयुक्तसीमाशुल्क(आयात) का कायाालय OFFICE OF THE PRINCIPAL COMMISSIONER OF CUSTOMS (IMPORT), हवाईमाल परिसि, सहाि, अंधेिी (पूवा), मुंबई - 400099 AIR CARGO COMPLEX, SAHAR, ANDHERI (E), MUMBAI – 400099 Email: Pro.acc-sahar@gov.in

PUBLIC NOTICE NO. 73/2025-26

Subject: Onboarding of CDSCO, WCCB, Textile Committee and MeitY on

SWIFT 2.0 as Single Touch Point for Trade. Attention of Importers, Customs Brokers and all other stakeholders is drawn towards Circular No. 05/2026-Customs dated 01.02.2026 read with Circular No. 29/2025-Customs dated 21.11.2025 issued by Ministry of Finance (Dept. of Revenue). 2. The Central Board of Indirect Taxes and Customs (CBIC) vide Circular No. 29/2025-Customs dated 21.11.2025 has envisaged to on board more than 60 Partner Government Agencies (PGAs) in a phased manner. As part of the first phase of rollout, three PGAs, namely AQCS, PQMS and FSSAI were on boarded on SWIFT 2.0 on pilot basis, and accordingly, consolidated lists of data fields/values and document requirements for AQCS, PQMS and FSSAI were finalized with the objective of providing a single touch point for EXIM clearances. At present, in order to have stakeholders’ feedback, AQCS unified application under SWIFT 2.0 is live for NOC processing at all ports; the PQMS unified application is live for NOC processing at Delhi and the FSSAI unified application is live for FSSAI ports including at Delhi and Kolkata Region.
3. In process of further deepening the scope of SWIFT 2.0, Board has decided to extend the same to two more PGAs, namely CDSCO and WCCB. Accordingly, the consolidated lists of data fields/values and document requirements for these PGAs have been formulated after inter-ministerial consultations involving Ministry of Health & Family Welfare and Ministry of Environment, Forest and Climate Change.

ocument requirements for these PGAs have been formulated after inter-ministerial consultations involving Ministry of Health & Family Welfare and Ministry of Environment, Forest and Climate Change. The detailed list of data fields, document codes and declarations for WCCB and CDSCO are annexed as Annexure-A and Annexure-B respectively, for reference. 4. In addition to this, at present, multiple Partner Government Agencies (PGAs) issue Licences, Permits, Certificates and Other Documents (LPCOs)/No Objection Certificates (NOCs) separately. In order to harmonize and streamline the filing and processing of such documents, a specific CUS/AG/PN/13/2025-PRO-O/o Commr-Cus-Imp-Zone-III-Mumbai I/3838749/2026 Dated: 10.02.2026

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document code has been assigned to each document issued by PGAs. These documents, mapped to the appropriate document codes, shall be brought under SWIFT 2.0. Accordingly, a set of new additional document codes of LPCOs/NOCs issued by various PGAs has been created and annexed as Annexure-C. Further, document codes used by trade for uploading documents have been created and attached as Annexure-D and two document codes issued vide Circular No. 03/2020-Customs dated 15.01.2020 are updated as annexed in Annexure-E. 5. Further, it is informed that the Ministry of Electronics and Information Technology (MeitY) and Textile Committee have been integrated into the SWIFT 2.0. The competent officers of MeitY and Textile Committee process the application in the Single Window environment.

on Technology (MeitY) and Textile Committee have been integrated into the SWIFT 2.0. The competent officers of MeitY and Textile Committee process the application in the Single Window environment. The Concessional Rate of Customs Duty Certificates (CCDC) and Compulsory Registration Order (CRO) exemption certificates issued by the MeitY shall be generated and accessed through the SWIFT 2.0 dashboard. These certificates shall be digitally integrated with the Bill of Entry for validation and record-keeping, thereby obviating the requirement for physical production of such certificates before Customs authorities. For the Textile Committee, importers may view Textile Committee test reports on the SWIFT dashboard, which shall also be made available to the proper Customs officer for cargo clearance, and may make payment of the prescribed fees through the single- touch-point interface. 6. Earlier, AQCS, CDSCO and WCCB were working on separate systems, but now in the present system, with an aim to provide single touch point for EXIM stakeholders and to reduce the dwell time, the PGA officers of AQCS, CDSCO and WCCB have been collocated onto the IT infrastructure systems of Indian Customs under SWIFT 2.0 for processing the NOCs. This would obviate the need for producing the documents separately before these authorities. 7. For further details on the subject matter, detailed Advisories will be issued by DG Systems/ICEGATE. The above functionalities will initially be made operational for obtaining feedback from the stakeholders prior to mandatory rollout. 8.

detailed Advisories will be issued by DG Systems/ICEGATE. The above functionalities will initially be made operational for obtaining feedback from the stakeholders prior to mandatory rollout. 8. Accordingly, five PGAs, namely FSSAI, AQCS, PQMS, WCCB and CDSCO, involved in Live Customs clearance will be progressively onboarded for complete integration under SWIFT 2.0 on or before 31.03.2026 suitably capturing the feedback of all stakeholders for this purpose. All PGAs will be onboarded in a phased manner by 31.03.2027. I/3838749/2026

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  1. Difficulties, if any, in implementation of this facility, may be brought to the notice of the Additional Commissioner of Customs, Technical (Import), ACC, Mumbai (email-pro.acc-sahar@gov.in). For assistance, clarification and information, the concerned importers may contact our Help Desk at TSK (Turant Suvidha Kendra) at email-tsk.accmumbaizone3@gov.in/Tel-022-

Hindi version follows.

(Manish Chandra)
Pr. Commissioner of Customs (Import) ACC, Mumbai. Copy:

  1. The Pr. Chief Commissioner of Customs, Mumbai Customs Zone –III, Mumbai.
  2. The Pr. Commissioner/Commissioner of Customs (General & Export), ACC, Mumbai.
  3. All Additional/Joint Commissioners of Customs (Import), ACC, Mumbai.
  4. All Additional/Joint Commissioner of Customs (General & Export), ACC, Mumbai.
  5. All Deputy/Assistant Commissioners of Customs (Import), ACC, Mumbai.
  6. Trade Associations
  7. CB Associations (BCBA)
  8. MIAL / Air India
  9. EDI section (for upload on Website)
  10. Office Copy

I/3838749/2026 SIGN

Commissioners of Customs (Import), ACC, Mumbai. 6. Trade Associations 7. CB Associations (BCBA) 8. MIAL / Air India 9. EDI section (for upload on Website) 10. Office Copy

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Annexure -A

  1. Data fields and Documents requirement for WCCB 1.1 List of Data Fields required by WCCB S. No . Data Field required by WCCB M/O in WCCB Mandatory/Conditional/Optional in BE 1 IEC M Mandatory 2 Custom House Code M Mandatory 3 Importer Name M Mandatory 4 Address of the Importer M Optional 5 Country of Origin M Mandatory 6 Supplier Country Name M Optional 7 Item No. M Mandatory 8 Invoice Sr. No. M Mandatory 9 Consignment Description M Mandatory 10 Gross quantity M Mandatory 11 HS Code M Mandatory 12 Value in Rupees (FOB/CIF/C & F) M Mandatory 13 Manufacture Name O Optional 14 Common name M Mandatory 15 Port of Entry M Mandatory 16 MAWB/BL No M Conditional (For Prior BE, this data field is Optional, otherwise mandatory.) 17 MAWB/BL Date M Conditional (For Prior BE, this data field is Optional, otherwise mandatory.) 18 IGM/ Arrival Date M Conditional (For Prior BE, this data field is Optional, otherwise mandatory.) 19 Gross Weight O Optional I/3838749/2026

a field is Optional, otherwise mandatory.) 18 IGM/ Arrival Date M Conditional (For Prior BE, this data field is Optional, otherwise mandatory.) 19 Gross Weight O Optional I/3838749/2026

20 Gross Weight Unit O Optional 21 Number of Packages O Optional 22 Package Code O Optional 23 Gateway IGM number M Conditional (For Prior BE, this data field is Optional, otherwise mandatory.) 24 IGM Date M Conditional (For Prior BE, this data field is Optional, otherwise mandatory.) 25 Invoice Date O Optional 26 Supplier Name M Mandatory 27 Supplier Address O Optional 28 Bill of Entry Number M Mandatory 29 Bill of Date M Mandatory 30 CFS Location M Not Available (This data field will be filed by the user in the Stage 2 – Mandatory Data field for Application, as the same is not being captured in BE filing.) 31 Mode of Entry / Shipment M Mandatory 32 Transit Country O Optional 33 Manufacturer Address O Optional I/3838749/2026

r Application, as the same is not being captured in BE filing.) 31 Mode of Entry / Shipment M Mandatory 32 Transit Country O Optional 33 Manufacturer Address O Optional I/3838749/2026

34 Scientific Name M Mandatory 35 CITES Permit No. O Optional (The user can file the Document Number in “Document Reference Number” data field while uploading in BE.) 36 CITES Permit Date O Optional (The user can file the Document Date in “Document Issue Date” data field while uploading the document in BE. (However, if the said document has been uploaded, then the Issue Date becomes Mandatory to be filed.) 37 CITES Permit Validity O Optional (The user can file the Seed dealer license valid up to in “Document Expiry Date” data field while uploading the document in BE.)

1.2 List of Documents required by WCCB S. No . Document Code Document Name Document Description Mandatory/Conditional/Optional 1. 331000 Invoice And Packing List Document/message serving as a preliminary invoice, containing - on the whole - the same information as then final invoice, but not actually claiming payment. Mandatory 2. 911000 Import License (DGFT)

Optional 6. 626000 Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) Certificate A certificate used in the trade of endangered species in accordance with the CITES convention. Optional 7.

ational Trade in Endangered Species of Wild Fauna and Flora (CITES) Certificate A certificate used in the trade of endangered species in accordance with the CITES convention. Optional 7. 626WC2 CITES Comparable Document for - Dalbergia sissoo CITES Comparable Document - Dalbergia sissoo issued by Wildlife Crime Control Bureau Optional I/3838749/2026

S. No . Document Code Document Name Document Description Mandatory/Conditional/Optional 8. 811WC1 Pre-Convention Certificate Pre-Convention Certificate is issued by Wildlife Crime Control Bureau if a specimen is procured before its being listed on CITES Optional 9. 861WC1 Country of Origin (Non- Preferential) Country of Origin (Non- Preferential) issued by Wildlife Crime Control Bureau Optional

1.3 List of Declarations required by WCCB S. No . Declaration Code Declaration title Declaration Description Mandatory/Conditional/Optional 1. WC001 Undertaking in case of an application to the Wildlife Crime Control Bureau I/We hereby undertake full responsibility in the detailed provided in this Bill of Entry and this shipment. Optional

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the Wildlife Crime Control Bureau I/We hereby undertake full responsibility in the detailed provided in this Bill of Entry and this shipment. Optional

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Annexure - B 2. Data fields and Documents requirement for CDSCO 2.1 List of Data Fields required by CDSCO S. No . Data Field required by CDSCO M/O in CDSCO Mandatory/Conditional/Optional in BE 1 Gateway IGM number M Conditional (For Prior BE, this data field is Optional, otherwise mandatory) 2 Consignment Description / Products name as per import permission / Variant Name M Mandatory 3 Exporting country O Optional 4 Port of Entry O Optional 5 Mode of Entry M Mandatory 6 Shipping/Airway Bill No. M Conditional (For Prior BE, this data field is Optional, otherwise mandatory) 7 Shipping/Airway Bill Date M Conditional (For Prior BE, this data field is Optional, otherwise mandatory) 8 Registration Certificate No. O Optional (The user can file the License Number in “Document Reference Number” data field while uploading the Registration certificate in BE.) 9 Registration Certificate Valid Up to O Optional (The user can file the License Number in “Document Reference Number” data field while uploading the Registration certificate in BE.) 10 Import License No. O Optional (The user can file the License Number in “Document Reference Number” data field while uploading the import License in BE.) I/3838749/2026

certificate in BE.) 10 Import License No. O Optional (The user can file the License Number in “Document Reference Number” data field while uploading the import License in BE.) I/3838749/2026

11 Import License Valid Up to O Optional (The user can file the License Number in “Document Reference Number” data field while uploading the import License in BE.) 12 Date of Lading M Conditional (For Prior BE, this data field is Optional, otherwise mandatory) 13 BE Number M Mandatory 14 BE Date M Mandatory 15 IE code M Mandatory 16 Importer Name M Mandatory 17 Importer Address O Optional 18 Country of Origin M Mandatory 19 Quantity M Mandatory 20 Units M Mandatory 21 CTH M Mandatory 22 Manufacturer Name O Optional 23 Exporter Name M Mandatory 24 Exporter Address O Optional 25 Invoice No M Mandatory 26 Invoice Value M Mandatory 27 Production Batch Identifier / Batch No. M Mandatory 28 Production Batch Quantity M Mandatory 29 Batch Quantity – Unit Quantity Code M Mandatory 30 Date of manufacturing M Mandatory 31 Date of Expiry M Mandatory 32 Best Before M Mandatory 33 Transit Country O Optional 34 Import Purpose M Mandatory I/3838749/2026

andatory 30 Date of manufacturing M Mandatory 31 Date of Expiry M Mandatory 32 Best Before M Mandatory 33 Transit Country O Optional 34 Import Purpose M Mandatory I/3838749/2026

35 CFS Location M Not Available (This data field will be filed by the user in the Stage 2 – Mandatory Data field for Application, as the same is not being captured in BE filing.) 36 Invoice Date O Optional 37 Container ID M Conditional (This data field is NOT required for AIR sites, X-bond BEs and SEZ T & M Type Bes. However, the same is Mandatory for Sea Shipments) 38 Port of loading M Mandatory 39 Port of unloading M Mandatory 40 Number of Packages O Optional 41 Manufacturer Address O Optional 42 Unit price M Mandatory 43 Total CIF Value O Optional 44 Brand name M Mandatory 45 CAS No. / IUPAC name where available O Optional 46 Composition of Finished Formulation /Cosmetics O Optional 47 Item Identification (GTIN) where available O Optional 48 Is it a Re-import M Mandatory 49 Drug Category M Mandatory I/3838749/2026

n of Finished Formulation /Cosmetics O Optional 47 Item Identification (GTIN) where available O Optional 48 Is it a Re-import M Mandatory 49 Drug Category M Mandatory I/3838749/2026

50 Whether Import for export/third country export (Declaration added – need to implement) M

2.2 List of Documents required by CDSCO S. No. Document Code Document Name Document Description Mandatory/Conditional/Opt ional 1. 101DC2

COS-4A - Import of already registered cosmetics into India. The Import Registration Number is issued by the CDSCO to authorize the import of cosmetics into India.
Conditional

Same as the Document Description 2. 9111DC Form 10 - License to import of drugs Form 10 under the CDSCO is an import license for drugs and cosmetics. Conditional

Same as the Document Description 3. 811DC4 Dual Use NOC- CDSCO

A Dual Use NOC from the CDSCO is required for importing or using substances that have Dual Use other than as a drug. Conditional

Same as the Document Description 4. 811DC6 MD-17 - License to Import Medical devices for purpose of clinical investigation or Test or Evaluation or Demonstration or Training. MD-17 test license to allows the import of small quantities of medical devices for specific purposes like testing, evaluation, training, or demonstration. Optional 5. 101DC1

Form 41 - Registration certificate for import of drugs into India under Drugs & Cosmetics rule 1945.

purposes like testing, evaluation, training, or demonstration. Optional 5. 101DC1

Form 41 - Registration certificate for import of drugs into India under Drugs & Cosmetics rule 1945. Registration Certificate (Drugs) issued by Central Drug Standards Control Organization (Form 41) Conditional

In BE, the said document is mandatory for CTH pertaining to Drugs 6. 101DC3 Cos-2 (Cosmetic)

  • Import registration certificate for Registration Certificate (Cosmetics) issued Conditional

In BE, the said document is I/3838749/2026

S. No. Document Code Document Name Document Description Mandatory/Conditional/Opt ional import of cosmetics into India. by Central Drug Standards Control Organization for first registration of Importer / Exporter (Form 43) mandatory for CTH pertaining to Cosmetics 7. 1010DC Registration Certificate
The Certificate issued by the Drug Controller General for the Drug Manufacturer Optional 8. 9111DC Import License for Drugs
Document/message issued by the Central Drug Standards Control Organization in accordance with import regulations in force by which authorization is granted to a named party to import either a limited quantity of designated articles or an unlimited quantity of such articles (Form 10) Optional 9. 911DC6

MD-15 Import License for Medical Device The license issued by the Drug Controller General for the Import of Medical Device Optional 10.

y of such articles (Form 10) Optional 9. 911DC6

MD-15 Import License for Medical Device The license issued by the Drug Controller General for the Import of Medical Device Optional 10. 911DC9

MD-19 License to import investigational Medical Device by Government hospital or statutory medical institution for the treatment of patients.

The license is issued by the Drug Controller General for the import of investigational Medical Device by Government hospital or statutory medical institution for the treatment of patients. Optional 11. 811DC5
MD-21 The license is issued by the Drug Optional I/3838749/2026

S. No. Document Code Document Name Document Description Mandatory/Conditional/Opt ional Permission to import of small quantity of Medical Devices for personal use Controller General for the import of small quantity of Medical Devices for personal use 12. 911DC5

Form-11 License to import drugs for the purpose of Examination, Test and Analysis The license is issued by the Drug Controller General for the import drugs for the purpose of Examination, Test and Analysis Optional 13. 911DC4

CT-17 License to Import new drugs for clinical trial or BA or BE study or for examination, test and analysis. The license is issued by the Drug Controller General for the Import new drugs for clinical trial or BA or BE study or for examination, test and analysis. Optional 14.

n, test and analysis. The license is issued by the Drug Controller General for the Import new drugs for clinical trial or BA or BE study or for examination, test and analysis. Optional 14. 911DC3

CT-25 License to Import or manufactured of unapproved new drugs for treatment of patients in Government hospital & Government medical institution. The license is issued by the Drug Controller General for the Import or manufactured of unapproved new drugs for treatment of patients in Government hospital & Government medical institution. Optional 15. 911DC2

Form 12B Permit for the Import of small quantities of drugs for personal use.
The license is issued by the Drug Controller General for the Import of small quantities of drugs for personal use. Optional 16. 331000 Invoice and Packing List Commercial invoice which includes a packing list Mandatory 17. 861000 Country of Origin Document/message identifying goods, in which the authority or body authorized Mandatory I/3838749/2026

mercial invoice which includes a packing list Mandatory 17. 861000 Country of Origin Document/message identifying goods, in which the authority or body authorized Mandatory I/3838749/2026

S. No. Document Code Document Name Document Description Mandatory/Conditional/Opt ional to issue it certifies expressly that the goods to which the certificate relates originate in a specific country. The word "country" may include a group of countries, a reg 18. 0010DC Certificate of analysis – Drug Certificate attesting to the quality or purity of the goods. Mandatory 19. 0030DC Batch Release Certificate (BRC) A Certificate confirming the release of a production batch after due testing and quality controls. Mandatory 20. 0110DC Label of Consignment Label of Consignment to be uploaded in imports by the IEC Holder or Customs Broker under Drugs and Cosmetics Act, 1940. Mandatory

  • This will be system calculated in officer dashboard 2.3 List of Fields required by CDSCO I. Drug Related Category – existing Qualifier (Info Qfr – DRC) –
    Note: Three information codes at Sl. Nos. 16, 17 and 18 have been added, and two codes have been removed, as detailed below. S. No Info Type Info Qfr Info code Info Description
  1. CTG DRC PER Items of personal use imported under a personal license
  2. CTG DRC NAR Items requiring clearance of the Central Bureau of Narcotics
  3. CTG DRC DUA Items of dual use imported under a dual use NOC issued by the respective zonal office
  4. CTG DRC EXC Excipients - items are excipients.

ance of the Central Bureau of Narcotics 3. CTG DRC DUA Items of dual use imported under a dual use NOC issued by the respective zonal office 4. CTG DRC EXC Excipients - items are excipients. These items require Declaration on intended use along with CAS details with category, IUPAC & International Proprietary name.
5. CTG DRC AYU Ayurvedic items
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  1. CTG DRC DNA DNA or rDNA products / Stem cells and cells-based products
  2. CTG DRC VAC Vaccines
  3. CTG DRC DEV Medical Devices
  4. CTG DRC HOM Homeopathy Drugs
  5. CTG DRC FIN Finished formulations
  6. CTG DRC NDK In vitro Diagnostic Kits
  7. CTG DRC COS Cosmetics
  8. CTG DRC BLD Blood Products
  9. CTG DRC BLK Bulk Drugs / API
  10. CTG DRC MSC Miscellaneous items do not fall under the above categories. These items require Declaration on intended use along with CAS details with category, IUPAC & International Proprietary name.
  11. CTG DRC OTR Others - KSM / Intermediate (To be added)
  12. CTG DRC VTF Veterinary Formulations (To be added)
  13. CTG DRC VTV Veterinary Vaccines (To be added)

Following info 2 codes removed
S. No Info Type Info Qfr Info code Info Description 1 CTG DRC HER Herbal Products (CDSCO-HQ- No Herbal is defined in the Act and Rules) 2 CTG DRC NNK Non-notified diagnostic kits

II. Drug Related Category – existing Qualifier (Info Qfr – GRA) S.

DRC HER Herbal Products (CDSCO-HQ- No Herbal is defined in the Act and Rules) 2 CTG DRC NNK Non-notified diagnostic kits

II. Drug Related Category – existing Qualifier (Info Qfr – GRA) S. No Info Type Info Qfr Info code Info Description 1 CTG GRA NFG Grade-Item not meant for human or animal consumption 2 CTG GRA PHG Item is pharma grade and or contains Active Pharmaceutical Ingredients (APIs) 3 CTG GRA NPH Item is not Pharma grade and does not contain Active Pharmaceutical Ingredients
(non-APIs)

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2.4 Proposed changes by CDSCO in declaration DC003
Letter of Guarantee to be submitted by the importer pending testing report, to avoid demurrage if the importer gives an undertaking in writing not to dispose of the drugs without the consent of Customs Commissioner etc., the goods can be released on L/G for test vide
Provision to Rule 40 of the Drugs Rules 1945. LETTER OF GUARANTEE FOR TEST

In consideration of the Commissioner of Customs or any Officer on his behalf having permitting to clear the above goods not withstanding his decision to detain the same goods under the above mentioned Rule 40 of the Drugs and Cosmetics Rules 1945 on having reason to doubt whether the above mentioned goods comply with the provisions of Chapter III of the Drugs & Cosmetics Act 1940 and rules there under. We hereby undertake –

  1. That we shall arrange for inspection of the goods as soon as they arrive in the godown and follow the instructions of representative of the O/o. Asstt.

ules there under. We hereby undertake –

  1. That we shall arrange for inspection of the goods as soon as they arrive in the godown and follow the instructions of representative of the O/o. Asstt. Drugs Controller (I), with regard to drawing of samples for test, rectification of labeling defects etc., if any.
  2. That we shall not dispose of the said goods without the consent of the Commissioner of Customs or any Officer on his behalf in writing.
  3. That we shall return the said goods in whole or in part as the Commissioner of Customs or any officer on his behalf may direct within ten days of receipt of a notice from the Commissioner of Customs or any officer on his behalf to return the goods.
  4. That we shall reship or surrender the said goods within two months of the receipt of any order to that effect from the Commissioner of Customs or any officer in his behalf. 5. That we shall forthwith pay such find and / or penalty and be liable for such punishment as the Commissioner of Customs or any Officer on his behalf or magistrate may impose under Section II of the drugs & Cosmetics Act, 1940 as read with the relevant provisions of the Customs Act, 1962 and Under Section 13 of the Drugs & Cosmetics Act, 1940.
    Any amount due under this bond may be recovered in the manner laid down in the subsection of the Section 142 of the Customs Act, 1962 without prejudice to any other mode or recovery.
    The undertakings referred to above is given in view of Rule 40 of the drugs and Cosmetics Rules 1945.
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2 of the Customs Act, 1962 without prejudice to any other mode or recovery.
The undertakings referred to above is given in view of Rule 40 of the drugs and Cosmetics Rules 1945.
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DC004 Letter of Guarantee submitted by the importer of drugs requiring cold storage such as sera, vaccines, may be released forthwith conditionally on L/G for test etc., for proper storage pending the completion of the formalities. -Letter of Guarantee (Direct Delivery)

  • vide Provision to Rule 40 of the Drugs & Cosmetic Rules, 1945. Letter of Undertaking for Test ( Direct Delivery)

In consideration of the Commissioner of Customs or any officer on his behalf having permitting to clear the above goods no with standing his decision to detain the same goods under the above mentioned Rule 40 of the Drugs and Cosmetics Rules 1945 on having reason to doubt whether the above mentioned goods comply with the provisions of Chapter III of the Drugs and Cosmetics Act 1940 and the Rules there under. We hereby undertake:

  1. That we shall arrange for inspection of the goods as soon as they arrive in our go-down by a representative of Astt. Drugs Controller (I) & obey his instructions as regards drawing samples under proper conditions and rectification of labeling defects if any etc.
  2. That we shall not dispose of the goods without the consent of the collector of Customs or any officer on his behalf in writing.

conditions and rectification of labeling defects if any etc. 2. That we shall not dispose of the goods without the consent of the collector of Customs or any officer on his behalf in writing. 3. That we return the said goods in whole or in part us the collector of Customs or any officer in his behalf direct within ten days of receipt of a notice from collector of Customs or any officer in his behalf to return the goods. 4. That we shall reship or surrender the said goods within two months of the receipt of any order to that effect from the Collector of Customs or any officer on his behalf. 5. That we shall forthwith pay such fine and/or penalty and be liable for such punishment as the collector of Customs or any
officer on his behalf or Magistrate may be impose under section II of the Drugs and Cosmetics Act, 1940 as red with the relevant provisions of the Customs Act, 1962 & under section 13 of the Drugs & Cosmetics Act, 1940.

Any amount due under this bond may be recovered in the, manner laid down in subsection of the section 142 of the Customs Act, 1962 without prejudice to any other mode of recover. The undertaking referred to above is given in view of Rule 40 of the Drugs & Cosmetics rules, 1945.
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n 142 of the Customs Act, 1962 without prejudice to any other mode of recover. The undertaking referred to above is given in view of Rule 40 of the Drugs & Cosmetics rules, 1945.
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DC007
Letter of Guarantee submitted by the importer where goods have been found to have labeling defects and importer desire to rectify the defects at their place, they may be allowed to be clear the consignment on L/G for rectification of labeling and/or test
For MEDICAL DEVICES: LABELING LETTER OF GUARANTEE FOR LABELING In consideration of the Commissioner of Customs or any officer on his behalf having permitted to clear the goods mentioned above, although the same have contravened the following provisions of the
Rule 44 of Medical Devices Rules, 2017 under Drugs & Cosmetics Act, 1940. We hereby undertake –

  1. That we shall label the goods mentioned above as required under the above rules within a month or such extended period as the Commissioner of Customs or any officer on his behalf may allow.
  2. That we shall not dispose of the said goods without the consent of the Commissioner of Customs or any officer on his behalf in writing.
  3. That we shall return the said goods in whole or in part us the Commissioner of Customs or any officer on his behalf nay direct within ten days of receipt of a notice from the Commissioner of Customs or any officer on his behalf to return the goods.

s the Commissioner of Customs or any officer on his behalf nay direct within ten days of receipt of a notice from the Commissioner of Customs or any officer on his behalf to return the goods. 4. That we shall reship or surrender the said goods within two months of the receipt of any order to that effect from the Commissioner of Customs or any Officer on his behalf. 5. That we shall forthwith pay such fine and /or penalty and be liable for such Punishment as the Commissioner of Customs or any Officer on his behalf or Magistrate may impose under Section II of the Drugs and Cosmetics Act, 1940 as red with the relevant provisions of the customs Act, 1962 and under Section 13 of the Drugs and Cosmetics Act, 1940. Any amount due under this bond may be recovered in the manner laid down in subsection of the Section 142 of the Customs Act, 1962 without prejudice to any other mode of recovery. The undertakings referred to above is given in view of Rule 44 of the Medical Devices Rule, 2017.
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on 142 of the Customs Act, 1962 without prejudice to any other mode of recovery. The undertakings referred to above is given in view of Rule 44 of the Medical Devices Rule, 2017.
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DC008
Letter of Guarantee submitted by the importer where goods have been found to have labeling defects and importer desire to rectify the defects at their place, they may be allowed to be clear the consignment on L/G for rectification of labeling and/or test. This is for COSMETICS LABELING. LETTER OF GUARANTEE FOR LABELING In consideration of the Commissioner of Customs or any officer on his behalf having permitted to clear the goods mentioned above, although the same have contravened the following provisions of the, Rule 34 of the Cosmetics Rules, 2020 under Drugs & Cosmetics Act, 1940. We hereby undertake –

  1. That we shall label the goods mentioned above as required under the above rules within a month or such extended period as the Commissioner of Customs or any officer on his behalf may allow.
  2. That we shall not dispose of the said goods without the consent of the Commissioner of Customs or any officer on his behalf in writing.
  3. That we shall return the said goods in whole or in part us the Commissioner of Customs or any officer on his behalf nay direct within ten days of receipt of a notice from the Commissioner of Customs or any officer on his behalf to return the goods.

s the Commissioner of Customs or any officer on his behalf nay direct within ten days of receipt of a notice from the Commissioner of Customs or any officer on his behalf to return the goods. 4. That we shall reship or surrender the said goods within two months of the receipt of any order to that effect from the Commissioner of Customs or any Officer on his behalf. 5. That we shall forthwith pay such fine and /or penalty and be liable for such Punishment as the Commissioner of Customs or any Officer on his behalf or Magistrate may impose under Section II of the Drugs and Cosmetics Act, 1940 as red with the relevant provisions of the customs Act, 1962 and under Section 13 of the Drugs and Cosmetics Act, 1940. Any amount due under this bond may be recovered in the manner laid down in subsection of the Section 142 of the Customs Act, 1962 without prejudice to any other mode of recovery. The undertakings referred to above are given in view of Rule 34 of the Cosmetics Rules, 2020.
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ection 142 of the Customs Act, 1962 without prejudice to any other mode of recovery. The undertakings referred to above are given in view of Rule 34 of the Cosmetics Rules, 2020.
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DC005 Letter of Guarantee submitted by the importer where goods have been found to have labeling defects and importer desire to rectify the defects at their place, they may be allowed to be clear the consignment on L/G for rectification of labeling and/or test

FOR DRUGS LABELING LETTER OF GUARANTEE FOR LABELING

In consideration of the Commissioner of Customs or any officer on his behalf having permitting to clear the goods mentioned above, although the same have contravened the following provisions of the Rules 40 and/or 96 (as applicable) of Drug Rules under Drugs & Cosmetics Act, 1940.

We hereby undertake –

  1. That we shall label the goods mentioned above as required under the above rules within a month or such extended period as the Commissioner of Customs or any officer on his behalf may allow.
  2. That we shall not dispose of the said goods without the consent of the Commissioner of Customs or any officer on his behalf in writing.
  3. That we shall return the said goods in whole or in part us the Commissioner of Customs or any officer on his behalf nay direct within ten days of receipt of a notice from the Commissioner of Customs or any officer on his behalf to return the goods.

s the Commissioner of Customs or any officer on his behalf nay direct within ten days of receipt of a notice from the Commissioner of Customs or any officer on his behalf to return the goods. 4. That we shall reship or surrender the said goods within two months of the receipt of any order to that effect from the Commissioner of Customs or any Officer on his behalf. 5. That we shall forthwith pay such fine and /or penalty and be liable for such Punishment as the Commissioner of Customs or any Officer on his behalf or Magistrate may impose under Section II of the Drugs and Cosmetics Act, 1940 as red with the relevant provisions of the customs Act, 1962 and under Section 13 of the Drugs and Cosmetics Act, 1940. Any amount due under this bond may be recovered in the manner laid down in subsection of the Section 142 of the Customs Act, 1962 without prejudice to any other mode of recovery. The undertakings referred to above is given in view of Rule 40 & 96 of the Drugs and Cosmetics Rules, 1945.
DC006
Undertaking for re- import of Drugs/Cosmetics/Medical Devices/API/Intermediate etc. I/We the exporter of this consignment undertake that the goods will be returned to the manufacturer concerned. I we/undertake that the re-imported material/product will be reexported only. No part of this consignment sold in India Market. I /We also undertake to produce an acceptance letter from the manufacturer to be obtained before release of goods. I/3838749/2026

xported only. No part of this consignment sold in India Market. I /We also undertake to produce an acceptance letter from the manufacturer to be obtained before release of goods. I/3838749/2026

Annexure - C 3. List of LPCOs/NOCs document codes issued by PGAs DOC CODE PGA Code DOC NAME DOC description DOC DESC 101AP6 APEDA Registration cum Allocation Certificate for the Export of “Basmati Rice”
Certificate is required for exporters dealing with products covered under the APEDA Act, including basmati rice.
101AP7 APEDA Certificate of Registration Integrated Abattoir-Cum-Meat Processing Plant A document that certifies that an integrated facility is approved for the hygienic and sanitary slaughtering and processing of animals for export 101AP8 APEDA Registration of Import contract for import of Sugar This certificate serves as permission to import sugar and allows the importer to proceed with the import process.
911AP1 APEDA Certificate of Export
A mandatory document for Indian exporters of agricultural and processed food products, signifying that their products meet international standards and that they are registered with the Agricultural and Processed Food Products Export Development Authority (APEDA) 101AQ1 AQCS Advance No Objection Certificate
An Advance No Objection Certificate (AQCS NOC) is a pre-arrival clearance document issued by India's Animal Quarantine and Certification Service (AQCS) to permit the import of live animals, such as pet dogs and cats 101AR1 ARAI Renewal of Recognition of

l clearance document issued by India's Animal Quarantine and Certification Service (AQCS) to permit the import of live animals, such as pet dogs and cats 101AR1 ARAI Renewal of Recognition of Scientific and Industrial Research Organisation (SIROs) Renewal of Recognition of Scientific and Industrial Research Organisation (SIROs) 101AR2 ARAI Certificate of Importer- Exporter Code Certificate of Importer-Exporter Code 101BIS BIS Registration Certificate A BIS Registration Certificate is an official authorization from the Bureau of Indian Standards (BIS), India's national standards body, certifying that a product meets specific Indian Standards and quality requirements 861CA2 CASHEW Certificate of Origin (Asia Pacific Trade Agrement (APTA)) The Certificate of Origin is a crucial document that verifies the country of origin of the cashew products for preferential treatment under the APTA trade agreement.
101BN2 CBN Manufacturing License A CBN manufacturing license is a legal authorization issued by India's Central Bureau I/3838749/2026

r preferential treatment under the APTA trade agreement.
101BN2 CBN Manufacturing License A CBN manufacturing license is a legal authorization issued by India's Central Bureau I/3838749/2026

of Narcotics (CBN) that permits a company to manufacture synthetic narcotic drugs 101BN3 CBN Quota Allocation for Narcotic Drugs The Central Bureau of Narcotics (CBN) issues annual quotas for the manufacture of narcotic drugs like medicinal opium and codeine. This quota system is designed to ensure a sufficient supply of these controlled substances for medical and scientific purposes while preventing their diversion for illicit use 101DC3 CDRUG Cos-2 (Cosmetic)

  • Import registration certificate for import of cosmetics into India. Registration Certificate (Cosmetics) issued by Central Drug Standards Control Organization for first registration of Importer / Exporter (Form 43) 101DC5 CDRUG Registration Certificate (Medical Devices) To get a Registration Certificate for a Medical Device from India's Central Drugs Standard Control Organisation (CDSCO), you must submit an online application through the SUGAM portal (Form MD-23) and provide required documents proving the device's safety and performance 101DC6 CDRUG MD import Licence Perpetual Under the Indian Medical Device Rules, 2017, import licenses for medical devices, issued in Form MD-15 by the CDSCO, are valid perpetually, meaning they do not have an expiry date 101DC7 CDRUG No Objection Certificate A Central Drugs Standard Control Organisation

l devices, issued in Form MD-15 by the CDSCO, are valid perpetually, meaning they do not have an expiry date 101DC7 CDRUG No Objection Certificate A Central Drugs Standard Control Organisation (CDSCO) No Objection Certificate (NOC) is a document required for the export of unapproved/approved new drugs from India, obtained through a streamlined online system that includes a one-time registration 811DC1 CDRUG Import (Test Licence for
Drugs) Under the Central Drugs Standard Control Organisation (CDSCO), a Test License for Imported Drugs allows the import of drugs for specific purposes like examination, testing, or analysis, and for clinical trials 811DC2 CDRUG Import (Test Licence for Medical device) To import a medical device for testing under the Central Drugs Standard Control Organisation (CDSCO) in India, you must apply for a test license via Form MD-16 on the Sugam portal, upload the required documents, pay the government fee, and submit the application online 811DC3 CDRUG FORM CT-16 CDSCO APPLICATION FOR GRANT OF LICENCE TO IMPORT NEW DRUG OR INVESTIGATIONAL NEW DRUG FOR CLINICAL TRIAL OR BIOAVAILABILITY OR BIOEQUIVALENCE STUDY OR FOR EXAMINATION, TEST AND ANALYSIS I/3838749/2026

PPLICATION FOR GRANT OF LICENCE TO IMPORT NEW DRUG OR INVESTIGATIONAL NEW DRUG FOR CLINICAL TRIAL OR BIOAVAILABILITY OR BIOEQUIVALENCE STUDY OR FOR EXAMINATION, TEST AND ANALYSIS I/3838749/2026

101003 CFFBD Receipt Letter Receipt Letter 101CH1 CHEMEXIL Receipt Letter Receipt Letter 911CI5 CIB Endorsement Certificate Certificate of Registration for pesticides that have been approved and meet the criteria outlined in the Insecticides Act, 1968 911CI6 CIB Free Sale Certificate Export document indicating that a product can be legally sold in the country of origin (India) and is not restricted for sale there 811DF1 DADF Permit import of LP by DAHDF To permit the import of livestock products (LOP) by the Department of Animal Husbandry and Dairying (DAHD), an applicant must obtain a Sanitary Import Permit (SIP) from the Department of Animal Husbandry and Dairying after an import risk analysis. This permit is issued for products listed under the DAHD's notification S.O. 2666(E) and must be secured before shipment. The permit is valid for a specified period, such as six months or a year, and allows for multiple consignments. Imports must go through designated sea/airports like Delhi, Mumbai, or Chennai, where animal quarantine and certification services are available.
101DE1 DAE License for Handling Prescribed Substances A DAE License for Handling Prescribed Substances is a mandatory certification required by the Department of Atomic Energy (DAE) and regulated by the Atomic Energy Regulatory Board (AERB) (AERB) in India.

cense for Handling Prescribed Substances is a mandatory certification required by the Department of Atomic Energy (DAE) and regulated by the Atomic Energy Regulatory Board (AERB) (AERB) in India. It grants permission to persons to mine, mill, process, and handle specific substances essential for atomic energy or related research, ensuring safety and compliance with the Atomic Energy Act of 1962 to protect public health and the environment.
911DE2 DAE License to Export Prescribed Equipment A DAE License to Export Prescribed Equipment is an authorization from India's Department of Atomic Energy (DAE) required to legally export items classified as "prescribed equipment" under the Atomic Energy Act 1962 101DG1 DGHS Customs Duty Exemption Certificate The Directorate General of Health Services (DGHS) in India issues Customs Duty Exemption Certificates (CDEC) for the import of life-saving drugs, drugs for rare diseases, and specialized medical equipment by hospitals and institutions, allowing for a reduced or nil rate of I/3838749/2026

ficates (CDEC) for the import of life-saving drugs, drugs for rare diseases, and specialized medical equipment by hospitals and institutions, allowing for a reduced or nil rate of I/3838749/2026

customs duty under specific government notifications 101EI1 EICI Certificate of Inspection/In- process Quality Control An EIC Certificate of Inspection/In-process Quality Control is a document issued by the Export Inspection Council (EIC) of India or its authorized agencies, certifying that an export consignment meets the quality, safety, and other requirements of the importing country and complies with India's Export (Quality Control and Inspection) Act, 1963 101EI2 EICI Health Certificate of Fish & Fishery Products (Frozen and Fresh/Chilled) Health Certificate of Fish & Fishery Products (Frozen and Fresh/Chilled) 101EI3 EICI Certificate of Inspection & Health Certificate of Dried Fish The EICI Certificate of Inspection & Health Certificate of Dried Fish is a combined document issued by India's Export Inspection Council (EIC) or its designated Export Inspection Agencies (EIAs) to certify that a consignment of dried fish meets quality, safety, and health standards for export, particularly to the European Union (EU) 101EI4 EICI Health certificate of Live Fish An EIC Health Certificate for Live Fish is an official document issued by India's Export Inspection Council (EIC) (or its designated Export Inspection Agencies) that certifies a consignment of live fish meets the health, safety, and quality standards required by the

y India's Export Inspection Council (EIC) (or its designated Export Inspection Agencies) that certifies a consignment of live fish meets the health, safety, and quality standards required by the importing country 861IE2 FIEO Preferential Certificate of Origin (APTA or SAPTA)* by DGFT A FIEO Preferential Certificate of Origin (APTA or SAPTA) is an official document issued by the Federation of Indian Export Organisations (FIEO) that certifies goods are from India and eligible for reduced tariffs under trade agreements like the Asia Pacific Trade Agreement (APTA) or the South Asian Preferential Trading Arrangement (SAPTA) 101HE2 HEPC For renewal of e-rcmc For renewal of e-rcmc 101MN1 MNRE Concessional custom duty certificate Document issued by India's Ministry of New and Renewable Energy (MNRE) to eligible manufacturers or project developers to allow for reduced import duties on specific raw materials or components 101MA1 MoCA Test Certificate
Test Certificate
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NRE) to eligible manufacturers or project developers to allow for reduced import duties on specific raw materials or components 101MA1 MoCA Test Certificate
Test Certificate
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101ME1 MoEFCC No Objection Certificate for Import of medical Equipment (Robotic Surgical Equipment) To obtain a No Objection Certificate (NOC) from the Ministry of Environment, Forest and Climate Change (MoEFCC) (HSM-Division) for importing Robotic Surgical Equipment, you must ensure the equipment is for reuse or refurbishment and comply with the Hazardous and Other Wastes (Management & Transboundary Movement) Rules, 2016 and the E-Waste (Management) Rules, 2022 101ME2 MoEFCC No Objection Certificate for Import of used test equipments (Hardware) To obtain a No Objection Certificate (NOC) from the Ministry of Environment, Forest and Climate Change (MoEFCC) HSM Division for importing used test equipment (hardware), an importer must submit a detailed report to the Ministry outlining the nature of the goods and their remaining useful life to ensure they are not considered e-waste 101ME3 MoEFCC No Objection Certificate for Import of Lead Scrap To obtain a No Objection Certificate (NOC) for the import of lead scrap, an applicant must submit a detailed application to the Hazardous Waste Management Division (HSM) of the Ministry of Environment, Forest and Climate Change (MoEFCC), following the guidelines under the Basel Convention and Indian regulations 101ME4 MoEFCC No Objection Certificate for Import of used Rubber tyres

ironment, Forest and Climate Change (MoEFCC), following the guidelines under the Basel Convention and Indian regulations 101ME4 MoEFCC No Objection Certificate for Import of used Rubber tyres To obtain a No Objection Certificate (NOC) for importing used rubber tires, an applicant must submit an online application to the MoEF&CC, which is reviewed by its Expert Committee (EC). The EC then requests the Central Pollution Control Board (CPCB) to inspect the applicant's premises. After the CPCB submits its site visit report, the MoEF&CC issues the Certificate for Import of used tires.
101ME5 MoEFCC No Objection Certificate for Import of used Oil To obtain a No Objection Certificate (NOC) for importing used oil from the Ministry of Environment, Forest and Climate Change (MoEFCC) in India, you must submit Form 5 under the Hazardous and Other Wastes (Management and Transboundary Movement) Rules, 2016, along with a detailed justification for import, a process flow chart, and an acknowledgement from the State Pollution Control Board (SPCB). This process ensures environmentally sound handling of the waste through a designated recycling facility I/3838749/2026

rt, and an acknowledgement from the State Pollution Control Board (SPCB). This process ensures environmentally sound handling of the waste through a designated recycling facility I/3838749/2026

101ME6 MoEFCC No Objection Certificate for Import of Polysiloxane waste and other e-waste for making various grades of silicon fluid To obtain a No Objection Certificate (NOC) for importing Polysiloxane waste and other e- waste for silicon fluid production from India's Ministry of Environment, Forest and Climate Change (MoEFCC), the importer must apply to the MoEFCC's Hazardous Waste Management (HSM) Division 101ME7 MoEFCC Permission for Export of e- waste To obtain permission for the export of e-waste from India,one must apply to the Ministry of Environment, Forest and Climate Change (MoEFCC), specifically the Hazardous and Other Wastes (Management and Transboundary Movement) Rules. 101MP2 MPEDA EU Catch Certificate The MPEDA EU Catch Certificate is a document issued by India's Marine Products Export Development Authority (MPEDA) to certify that marine products exported from India to the European Union (EU) are legally caught and harvested, thereby combating Illegal, Unreported, and Unregulated (IUU) fishing 101MP3 MPEDA Non - EU Catch Certificate The MPEDA Non-EU Catch Certificate is a digital document issued by India's Marine Products Export Development Authority (MPEDA) to certify that marine products exported to European Union (EU) countries are caught legally and have not been subjected to Illegal,

India's Marine Products Export Development Authority (MPEDA) to certify that marine products exported to European Union (EU) countries are caught legally and have not been subjected to Illegal, Unreported, and Unregulated (IUU) fishing practices 101MP4 MPEDA COO MPEDA A Certificate of Origin (CoO) issued by MPEDA is a document that verifies the country where marine products exported from India originate 101MP5 MPEDA Non Radio-Activity Certificate An MPEDA Non Radio-Activity Certificate is a document issued by the Marine Products Export Development Authority (MPEDA) of India, certifying that a shipment of fish and fishery products, caught in Indian waters, is free from radioactive contamination or contains only acceptable trace amounts, meeting the requirements of importing countries 101MP6 MPEDA Duty free Import Certificate A MPEDA Duty Free Import Certificate is an attestation by the Marine Products Export Development Authority (MPEDA) that certifies an exporter's past export quantity and value for a specific year, enabling them to avail a 1% duty benefit on the Free On Board (FOB) value I/3838749/2026

opment Authority (MPEDA) that certifies an exporter's past export quantity and value for a specific year, enabling them to avail a 1% duty benefit on the Free On Board (FOB) value I/3838749/2026

for importing goods under the relevant Customs Notification 911MP1 MPEDA Exporter Certificate Application MPEDA The MPEDA registration and certificate are essential for marine product exporters in India to comply with regulations, gain access to financial subsidies and licenses, and participate in marketing activities designed to promote the sector.
861SF2 SFPEPC Country of Origin certificate (COO) A Country of Origin Certificate (COO) issued by the Shellac and Forest Products Export Promotion Council (SHEFEXIL) is an official document confirming that a specific forest- based product, such as shellac, guar gum, or sesame seeds, originates from India 101SB2 SPICE Certificate of Registration as Exporter of Spices (CRES) The Certificate of Registration as Exporter of Spices (CRES) is a mandatory license issued by the Spices Board of India for all businesses engaged in exporting spices from India 101SB3 SPICE Mandatory Sampling & Testing for export of spices & spice products The SPICE Board's mandatory sampling and testing for spice exports ensures safety and quality by requiring exporters to submit samples to the Board's Quality Evaluation Laboratories (QELs) or accredited facilities for testing, often including pesticide residue analysis, mycotoxins, and microbial contaminants 101SB4 SPICE Registration as Exporter

y Evaluation Laboratories (QELs) or accredited facilities for testing, often including pesticide residue analysis, mycotoxins, and microbial contaminants 101SB4 SPICE Registration as Exporter under REX self-certification system The REX self-certification system for the Spices Board (SPICE) is the Registered Exporter (REX) system, an European Union (EU) initiative that allows exporters to self-certify the origin of their goods, replacing the need for public authorities to issue a certificate of origin 101SB5 SPICE SAMPLE DRAWN CERTIFICATE
SAMPLE DRAWN CERTIFICATE
101SB6 SPICE Yield Recommendation
The "Spices Board SPICE Yield Recommendation" refers to the guidance provided by the Spices Board of India, under its Spice Productivity, Improved Cultivation & Enhancement (SPICE) scheme, for increasing crop yields through recommendations such as adopting high-yielding varieties, using improved planting materials, implementing proper irrigation and fertigation practices, managing pests and diseases with Integrated Pest Management (IPM), and ensuring better post-harvest management I/3838749/2026

aterials, implementing proper irrigation and fertigation practices, managing pests and diseases with Integrated Pest Management (IPM), and ensuring better post-harvest management I/3838749/2026

636SB1 SPICE Health Certificate A Spices Board Health Certificate is an official document issued by the Spices Board of India to an authorized exporter, confirming that a spice consignment meets health and quality standards for export, often a prerequisite for specific destinations like the EU and UK for certain products like chilli, nutmeg, and their derivatives 861SB1 SPICE COO for spices COO for spices
101SR2 SRTEPC Current Shipment Request Current Shipment Request 861SR2 SRTEPC Certificate of Origin
The Synthetic & Rayon Textiles Export Promotion Council (SRTEPC) Certificate of Origin is a document issued by the Indian government, through the Ministry of Textiles, to confirm the country of origin for synthetic and rayon textiles being exported from India 911SR4 SRTEPC Export Performance Certificate (EPC) The Synthetic & Rayon Textiles Export Promotion Council (SRTEPC) issues an Export Performance Certificate (EPC) to its eligible member-exporters based on their annual export figures. The certificate is used to avail benefits under various government schemes, such as importing raw materials at a concessional duty rate.

le member-exporters based on their annual export figures. The certificate is used to avail benefits under various government schemes, such as importing raw materials at a concessional duty rate. 911SR5 SRTEPC Export Turnover Certificate Export Turnover Certificate 101ST1 STC 101TB1 TBDI Business License for Carrying Business as Distributor A "Tea Board Business License for Carrying Business as Distributor" is a required legal permit in India for businesses that distribute tea and tea products. This Tea Board license from the Tea Board of India, often referred to by an identifier like "TBDI" (Tea Board of India), ensures compliance with quality standards and regulations, building trust with consumers and partners 101TO5 TOBBD Form of certificate of registration as processor or manufacturer of Virginia tobacco/as exporter of tobacco (Form 14) Certificate of Registration itself for processing, manufacturing, or exporting Virginia tobacco issued by Tobacco Board I/3838749/2026

urer of Virginia tobacco/as exporter of tobacco (Form 14) Certificate of Registration itself for processing, manufacturing, or exporting Virginia tobacco issued by Tobacco Board I/3838749/2026

101WP1 WPC The Equipment Type Approval Certificate Certificate required for the import, sale, and use of wireless communication devices that operate in de-licensed frequency bands or involve radio frequency (RF) transmission 101WP3 WPC Decision to grant W/T License (New/Additional/Revised) Decision to grant W/T License (New/Additional/Revised) 101WP4 WPC Issue Wireless Station License Issue Wireless Station License 101WP5 WPC Wireless Station License Authorization Wireless Station License Authorization 811WP2 WPC License to Import Wireless Transmitting and / or Receiving Apparatus into India Certifies that a wireless product's design complies with Indian radio frequency (RF) standards, including operating in de-licensed bands.

s Transmitting and / or Receiving Apparatus into India Certifies that a wireless product's design complies with Indian radio frequency (RF) standards, including operating in de-licensed bands. AQ0013 AQCS (NOC) -issued by AQCS No Objection Certificate - NOC issued by AQCS 1010DC CDRUG Registration Certificate The Certificate issued by the Drug Controller General for the Drug Manufacturer
811DC4 CDRUG Dual Use NOC A dual use NOC from CDSCO is required for importing or using substances that have dual use other than as a drug 811DC5 CDRUG MD-21 The license is issued by the CDSCO for import of small quantity of medical devices for personal use CDSCO1 CDSCO (NOC)-issued by CDSCO No Objection Certificate - NOC issued by CDSCO 101ES1 ECSEPC Registration cum Membership Certificate Registration cum Membership Certificate issued by Electronic and Computer Software Export Promotion Council for availing benefits under Foreign Trade Policy FSS015 FSSAI (NOC)-Issued by FSSAI No Objection Certificate - NOC issued by FSSAI 911EA1 MEA Customs Duty Exemption Certificate (CDEC) Customs Duty Exemption Certificate issue by MEA 104PQ1 PQMS (NOC) - issues by PQMS No Objection Certificate - NOC issued by PQMS WCCB01 WCCB (NOC)- Issued by WCCB No Objection Certificate - NOC issued by WCCB 811DC6 CDRUG MD-17 License to Import Medical devices for purpose of clinical investigation or Test or Evaluation or Demonstration or Training. I/3838749/2026

Certificate - NOC issued by WCCB 811DC6 CDRUG MD-17 License to Import Medical devices for purpose of clinical investigation or Test or Evaluation or Demonstration or Training. I/3838749/2026

911LE3 CLE Certificate for availing Bank Guarantee Exemption under EPCG/AA Certificate for availing Bank Guarantee Exemption under EPCG/AA issued by CLE 911LE4 CLE Import of footwear soles into India for production or assembly of footwear for exports purposes Import of footwear soles into India for production or assembly of footwear for exports purposes issued by CLE

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Annexure - D

Document codes for trade
S.NO DOC CODE DOC NAME DOC DESC 1 AQ0001 Vaccination Book Historical vaccination data of the Animal 2 AQ0002 Passport of Owner Importer and Pet owner have to be the same person 3 AQ0003 Visa of Owner Importer and Pet owner have to be the same person 4 AQ0004 Employment Details Employment details to be provided, in order to utilise the baggage rules 5 AQ0005 Transfer of Residence Proof Employment details to be provided, in order to utilise the baggage rules 6 AQ0006 Proof of regular 2 year stay abroad Employment details to be provided, in order to utilise the baggage rules 7 AQ0007 Journey Ticket Journey ticket of the Importer 8 AQ0009 Return ticket Journey ticket of the Importer 9 AQ0010 Proof of purpose of visit Declaration of the Importer - exhibition / events 10 AQ0011 Local / Temporary address Declaration from the local person to take the responsibility

porter 9 AQ0010 Proof of purpose of visit Declaration of the Importer - exhibition / events 10 AQ0011 Local / Temporary address Declaration from the local person to take the responsibility of that pet otherwise that person will be held responsible 11 101PAY Payment receipt Receipt generated post payment by user 12 101004 (New Addition)
Any other document Others

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Annexure - E

  1. Updation in document codes issued through Circular 03/2020- Customs dated 15.01.2020. Note: The following two document codes, which were already published vide Circular No. 03/2020-Customs dated 15.01.2020, have been updated. Sr.No. Current DOC_Code DOC_Name DOC_DESC PGA_Code Circular reference Proposed updated code 13 911DA1 Import Licence Licence for import is issued by Department of Atomic Energy for import of prescribed substance as per Atomic energy Act, 1962 and Rules thereunder Department of Atomic Energy (DAE) Circular 03/2020- Customs dated 15.01.2020 911DE1 14 811DA1 Export licence Licence for Export is issued by Department of Atomic Energy for Export of prescribed substance as per Atomic Energy Act, 1962 and Rules thereunder Department of Atomic Energy (DAE) Circular 03/2020- Customs dated 15.01.2020 811DE1

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