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of <h1>EPCG Authorization Form Updated: Drug Licence Details Removed, New Declaration for Pharma Exports Introduced in Handbook Amendment.</h1> The Director General of Foreign Trade has amended the Handbook of Procedures (Vol.1) regarding the EPCG Authorization (ANF-5A). The amendments include the removal of the requirement for Drug Manufacturing Licence details in the application form. Applicants must now provide a self-certified copy of IEM/SSI registration for products and Service Tax Registration for service providers, unless exempted. A new declaration mandates submission of a Drug Manufacturing Licence within three years for pharmaceutical exports, failing which the Bank Guarantee or Legal Undertaking may be forfeited, and Customs Duty with interest will be due. These changes are implemented in public interest.
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