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of <h1>New Guidelines for Tracking Duty-Free Raw Materials in Pharma Manufacturing Under Advance Authorization, Section 25% Solvent Rule Applies.</h1> The procedure for maintaining a register to account for the consumption and stocks of duty-free imported or domestically procured raw materials and components used under advance authorization for manufacturing pharmaceutical products through a Non-Infringing (NI) process. It includes details such as authorization numbers, input names and quantities, product names, and quantities exported. It requires declarations of accuracy from authorization holders and certification by a Chartered Engineer or Customs official. The document specifies that solvents are allowed up to 25% of the requirement unless recovery is impossible, in which case full quantities are permitted.
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