Shipping Pharma Products from Baltimore to Rotterdam via Air Freight

Transporting temperature-sensitive pharmaceutical goods demands Validated insulated packaging, suitable refrigerants, and maintained temperature monitoring. Specify an express service where possible, pre-cool gel packs, and Add 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 compartmental inserts with Top and bottom cushioning. Set trays inside a sturdy shipping box and stabilize using void-fill so nothing moves. For moisture-sensitive medical drugs, pair this with moisture-barrier inner bags and desiccants.

International shipments of medical drugs typically necessitate a detailed commercial invoice, packing list, and any permits 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. Verify requirements with your customs broker before shipping.

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

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

The documentation for shipping pharmaceuticals includes a commercial invoice, packing list, air waybill, and any specific certificates required by the Netherlands, such as a Certificate of Analysis or GMP compliance. Additionally, import permits may be necessary depending on the type of pharmaceuticals being shipped.

Yes, shipping pharmaceuticals from the United States to the Netherlands requires compliance with both U.S. FDA regulations and European Medicines Agency (EMA) guidelines. This includes ensuring that the pharmaceuticals meet safety, efficacy, and quality standards, as well as proper labeling and packaging requirements.

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.