Shipping Medical Drugs from Rio de Janeiro to Newark via Air Freight

Shipping temperature-sensitive medicines necessitates Validated insulated packaging, correct refrigerants, and unbroken temperature monitoring. Specify an express service where possible, stabilize 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 Medicines must be packed in cell dividers with Top and bottom cushioning. Position trays inside a double-walled box and stabilize using void-fill so nothing moves. For moisture-sensitive medical drugs, integrate this with moisture-barrier inner bags and desiccants.

International shipments of Pharmaceutical goods typically demand a detailed commercial invoice, packing list, and any authorizations required by the importing country. Many destinations also require 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 Medicines, select moisture-proof inner liners plus desiccant sachets inside the packaging. Seal cartons tightly, avoid damaged boxes, and book transport options that reduce exposure to rain and high humidity, such as covered docks and climate-controlled linehaul for medical drugs.

High-value Pharma products generally need tailored cargo insurance that covers temperature excursions, breakage, and theft. Work with an insurer familiar with pharmaceutical goods, state 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 and careful handling to prevent damage. It is essential to use validated packaging that maintains the required temperature and protects the integrity of the products during transit.

Required documentation includes a commercial invoice, packing list, certificate of origin, and any specific regulatory documents related to pharmaceuticals, such as FDA approval or import permits, to comply with U.S. customs regulations.

We combine smarter tech—through the SAMMIE AI platform—with faster answers and people who truly care, including dedicated Client Success Officers, so customers get both advanced visibility and hands-on, proactive support.

Most customers are up and running within days, after we gather basic shipment details and compliance documents, set up your profile, configure SAMMIE access, and align your first shipment.

Most platforms only show carrier data, while SAMMIE is built on ecosystem data from third-party sources and DNA’s proprietary history, enabling predictive ETAs, intelligent alerts, and advanced automation powered by clean, validated data.