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Angelina Fletcher
Guest
When importing infusion products, compliance with regulations is crucial. In the U.S., infusion products must be FDA-approved, with proper documentation such as a Certificate of Free Sale. Infusion importers also need to follow customs requirements, which involve accurate classification, valuation, and labeling to avoid delays or fines. Adhering to Good Manufacturing Practice (GMP) standards is essential to ensure consistent quality. Additionally, some countries require specific licenses or permits for importing medical products, so checking with local authorities is necessary to obtain all required permits.