Comprehensive guide for importers detailing procedures for submitting the Single Import Declaration (DUIMP) through the Single Foreign Trade Portal. Covers documentation requirements (commercial invoice, bill of lading), regulatory compliance (GMP certificates, quality control reports), import categories (direct, on account, by order), sanitary inspections, product catalog attributes, and special cases for products not regularized by ANVISA. Version 1.7 includes updates on storage facility CNPJ, TIN number, product name, regulatory category, composition, shelf life, CAS number, and sanitary risk management.
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