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Direct-to-patient and decentralized trial logistics under FDA guidance and ICH E6(R3) Annex 2, effective January 2027. What sponsors must do now.

See how a dedicated account manager and operations squad give healthcare shippers one point of contact, proactive tracking, and faster fixes.

Learn how to get a US import license or permit, which federal agencies require them, and the step-by-step application process for regulated goods.

Compare the best temperature-controlled shipping containers for pharma, biologics, and clinical trials, including passive and active options.

Compare ATA Carnets and temporary import bonds (TIB): how each works, which to choose, country coverage, timelines, and penalties to avoid.

Learn how to build and ship compliant IMP kits for clinical trials. Covers GMP assembly, EU CTR labeling, cold chain, blinded packaging, and depot logistics.

Learn how to ship DEA-scheduled substances compliantly. This guide covers registration, Form 222, carrier authorization, and chain of custody for lab teams.

DSCSA 2026 requires full electronic traceability across pharma supply chains. Learn what shippers must do now to stay compliant before enforcement begins.

Meet Colin Brady, Mercury's Director of Business Development. With 15+ years in healthcare logistics, he brings deep operational and commercial expertise.

American Expediting closed on June 3, 2026. If your supply chain depends on a single provider, here is what to do now and how to prevent future disruption.