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of <h1>New Format for Tracking Duty-Free Raw Materials & Components in Pharmaceutical Manufacturing Under Advance Authorization</h1> The format for accounting the consumption and stocks of duty-free imported or domestically procured raw materials and components used under advance authorization for pharmaceutical products manufactured through a Non-Infringing (NI) process. It includes details such as the authorization number, input names, quantities, and consumption data. The format requires signatures and official details of the authorization holder. A Central Excise Certificate is necessary to verify the production details and input consumption for exported pharmaceutical products. Specific provisions for solvent usage are also included, with verification by Central Excise Authority.
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