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

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..... ed under advance authorisation for pharmaceutical product manufactured through Non Infringing (NI) process. inputs allowed in the authorisation Product (s) exported under the authorisation Balance inputs, if any In case of balance inputs as in column 9 remarks Sl.No. Authorisation No(s) with date Name of the Inputs Quantity Name of the Product Quantity Inputs Actually consumed for the .....

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..... ___ Note: 1. Please mention N.A. wherever the information required in the table is not applicable. 2. For columns 10 & 12 of the 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 details furnished in Ap .....

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..... any): Postal Address: Note: 1. This certificate shall be required only when the product manufactured and exported is a pharmaceutical product manufactured through Non-Infringing (NI) process. This certificate is to be signed by an official not below the rank of Superintendent of Central Excise, under whose jurisdiction the manufacturing unit of the Advance Authorisation holder is located). 2. .....

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