Shipping Pharma Products from Kobe to New Orleans via Ocean Freight

Transporting temperature-sensitive pharmaceutical goods Requires tested thermal shippers, suitable refrigerants, and unbroken temperature monitoring. Use an express service where possible, Pre-condition gel packs, and place a data logger in the carton to verify that medical drugs stayed within their labeled temperature range.

Fragile glass vials of pharmaceutical goods need to be packed in Molded trays with 360-degree padding. Set trays inside a double-walled box and Fill void-fill so nothing moves. For moisture-sensitive medical drugs, Combine this with moisture-barrier inner bags and desiccants.

International shipments of medical drugs typically necessitate a detailed commercial invoice, packing list, and any Licenses required by the importing country. Most regulated markets also ask for Certificates of Analysis, proof of GDP-compliant handling, and clear temperature instructions for cold-chain medicines. Double-check requirements with your customs broker before shipping.

For moisture-sensitive pharmaceutical goods, specify Foil-laminate pouches plus desiccant sachets inside the packaging. Secure cartons tightly, avoid damaged boxes, and select transport options that reduce exposure to rain and high humidity, such as covered docks and climate-controlled linehaul for medical drugs.

High-value medical drugs usually require Specialized cargo insurance that covers temperature excursions, breakage, and theft. Consult an insurer familiar with pharmaceutical goods, specify the full replacement value, and retain temperature and handling records so claims can be processed efficiently if something goes wrong.

Pharmaceuticals require temperature-controlled environments during transit to maintain efficacy. Proper packaging and insulation materials must be used to ensure compliance with temperature regulations throughout the journey. Additionally, specific handling procedures should be followed to minimize risk of contamination or damage.

When importing pharmaceuticals into the United States, compliance with the FDA regulations is essential. Importers must ensure that all products are registered and approved by the FDA, and appropriate documentation, such as a Certificate of Analysis and import permits, must be provided to customs upon arrival in New Orleans.

Yes, our team is able to integrate via robust EDI/API capabilities, mapping fields, automating status updates, pushing documentation, and syncing PO and invoice data with systems like SAP, NetSuite, Oracle, or custom WMS/ERP platforms.

Yes, our system supports user-level permissions so warehouse, finance, purchasing, or customer service teams can access exactly what they need and nothing they don’t.

Yes, our in-house team provides this. Our licensed customs experts handle import/export compliance, HS classification, tariff codes, ISF filings, and coordination with U.S. and international agencies.