Shipping Pharma Products from Baltimore to Amsterdam via Air Freight

Transporting temperature-sensitive Pharma products Requires Validated insulated packaging, suitable refrigerants, and Continuous temperature monitoring. Use an express service where possible, stabilize gel packs, and include a data logger in the carton to verify that medical drugs stayed within their labeled temperature range.

Fragile glass vials of pharmaceutical goods Should be packed in Molded trays with Top and bottom cushioning. Set trays inside a Rigid outer carton and Fill void-fill so nothing moves. For moisture-sensitive medical drugs, integrate this with moisture-barrier inner bags and desiccants.

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

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

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

Pharmaceuticals require strict temperature control and monitoring throughout the shipping process to maintain product integrity. It is essential to use validated temperature-controlled packaging and ensure compliance with both U.S. and EU regulations regarding the transport of medical goods.

Shipping pharmaceuticals requires specific documentation, including a commercial invoice, a certificate of analysis, and any necessary import permits. Additionally, compliance with EU regulations on medicinal products is mandatory, which may involve providing a summary of product characteristics and safety data sheets.

Yes, one example is CE North America, where we built a custom EDI feed that pushes real-time shipment updates, documentation, and exception alerts directly into their ERP, eliminating dozens of manual tasks and improving cross-department visibility.

Yes, DNA offers full port-to-door service, managing booking, loading, customs clearance, and final-mile delivery with one point of contact and one visibility platform.

Yes, our credentials are viewable. You can see our certifications and compliance credentials, including FMC license, DOT number, and C-TPAT partnership, in the Certifications section of our FAQs.