Document text
To
F. No.450/12/2026-CUS IV
Government of India
Ministry of Finance,
Department of Revenue
Circular No. 05/2026-Customs
(Central Board of Indirect Taxes & Customs)
Room No.16049, 6th Floor
Kartavya Bhawan-1, New Delhi
Dated: 1st February 2026
The
Principal
Chief
Commissioners/Chief
Commissioner
of Customs/Customs
(Preventive)/Customs & Central Tax,
The Principal Commissioners/Commissioners of Customs/Customs (Preventive)/Customs &
Central Tax,
The Principal Director Generals/Director Generals under CBIC
Subject: Onboarding of COSCO, WCCB, Textile Committee and MeitY on SWIFT 2.0
as Single Touch Point for Trade - reg.
Kind reference is invited to Board Circular No. 29/2025-Customs dated 21.11.2025
regarding the launch of SWIFT 2.0, wherein it was envisaged to onboard 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 onboarded on SWIFT 2.0 on
pilot basis, and accordingly, consolidated lists of data fields/values and document
requirements for AQCS, PQMS and FSSAI were finalised 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.
2.
In the process of further deepening the scope of SWIFT 2.0, it has now been decided
to extend the same to two more PGAs, namely COSCO and WCCB. Accordingly, the
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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. The detailed list of data
fields, document codes and declarations for WCCB and COSCO are annexed as Annexure-A
and Annexure-B respectively, for reference.
3.
In addition to this, at present, multiple Partner Government Agencies (PG As) issue
Licences, Permits, Certificates and Other Documents (LPCOs)/No Objection Certificates
(NOCs) separately. In order to harmonise and streamline the filing and processing of such
documents, a specific document code has been assigned to each document issued by PGAs.
These documents, mapped to the appropriate document codes, shall be consumed 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.
4.
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. 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.
5.
Earlier, AQCS, COSCO and WCCB were working on separate systems, 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.
6.
DG Systems is advised to issue a detailed advisory in respect of all PGAs integrated
under SWIFT 2.0. The above functionalities shall initially be made operational for obtaining
feedback from the stakeholders prior to mandatory rollout.
7.
Accordingly, five PGAs, namely FSSAI, AQCS, PQMS, WCCB and CDSCO,
involved in live Customs clearance shall 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.
8.
Field formations are requested to issue suitable Public Notices/Trade Notices to
sensitise stakeholders and ensure correct and complete filing of data and documents under
SWIFT 2.0.
9.
Any difficulties in implementation may be brought to the notice of the Board at the
earliest.
Hindi version follows.
Enclosure: As above
Yours faithfully,
(Suresh umar Meena)
Deputy Commissioner/OSD
Customs Policy Wing
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
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
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.
626WC2
CITES
Comparable
Document for -
Dalbergia sissoo
CITES Comparable
Document - Dalbergia
sissoo issued by Wildlife
Crime Control Bureau
Optional
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
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.)
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
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
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.
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
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. 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
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. 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
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. These items require Declaration
on intended use along with CAS details with category, IUPAC &
International Proprietary name.
5. CTG
DRC
AYU
Ayurvedic items
6. CTG
DRC
DNA
DNA or rDNA products / Stem cells and cells-based products
7. CTG
DRC
VAC
Vaccines
8. CTG
DRC
DEV
Medical Devices
9. CTG
DRC
HOM
Homeopathy Drugs
10. CTG
DRC
FIN
Finished formulations
11. CTG
DRC
NDK
In vitro Diagnostic Kits
12. CTG
DRC
COS
Cosmetics
13. CTG
DRC
BLD
Blood Products
14. CTG
DRC
BLK
Bulk Drugs / API
15. 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.
16. CTG
DRC
OTR
Others - KSM / Intermediate (To be added)
17. CTG
DRC
VTF
Veterinary Formulations (To be added)
18. 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.
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)
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. 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.
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.
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.
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.
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.
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.
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.
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.
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.
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
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
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
(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
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. 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
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
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
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
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
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,
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
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
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
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.
911SR5
SRTEPC
Export Turnover Certificate
Export Turnover Certificate
101ST1
STC
No Objection Certificate
No Objection Certificate
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
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.
AQ0013
AQCS
No Objection Certificate
(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
No Objection Certificate
(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
No Objection Certificate
(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
No Objection Certificate
(NOC) - issues by PQMS
No Objection Certificate - NOC issued by PQMS
WCCB01
WCCB
No Objection Certificate
(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.
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
Annexure - D
4.
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
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
Annexure - E
5. 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
