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Advance authorisation for pharmaceutical product manufactured through Non Infringing (NI) process

Appendix -4I - Procedure - Appendix - Foreign Trade Procedure 2015-2020 (From 5-12-2017 to 31-3-2020) Revised - Appendix -4I - APPENDIX - 4 I (Please see Para 4.18 to 4.21 of HBP) Register for accounting of consumption and stocks of duty free importe .....

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(s) with date Name of the Inputs Quantity Name of the Product Quantity Inputs Actually consumed for the exported product ** (4 - 8) Additional exports effected in proportion to excess inputs Input quantity reduced proportionately in the authorisation .....

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of inputs used (whether duty paid or not) in the exported product has to be furnished. We declare that the aforesaid particulars are correct. Place: Signature of the authorisation holder__________ Date: Name in block letters:____________ Full officia .....

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he table, please furnish the copy of the documentary evidence. FORMAT OF CENTRAL EXCISE CERTIFICATE I hereby confirm that I have examined the production details and the records of M/s __________(Name of the authorisation holder) and verified the deta .....

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e Advance Authorisation holder: 2. Address of the manufacturing unit: 3. Name of the exported product: 4. Type of exports: Physical / Deemed / Both (pl strike out whichever is not applicable). 5. Period for which production details verified: 6. Quant .....

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