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市场调查报告书
商品编码
1934782
美国医学流:市场占有率分析、产业趋势与统计、成长预测(2026-2031)United States Pharmaceutical Logistics - Market Share Analysis, Industry Trends & Statistics, Growth Forecasts (2026 - 2031) |
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2025年美国医药物流市场价值为759.6亿美元,预计到2031年将达到926.7亿美元,高于2026年的785.3亿美元。
预计在预测期(2026-2031 年)内,复合年增长率将达到 3.38%。

美国药品物流市场规模预测报告重点指出,合规期限和生物製药需求正在重塑成本结构和服务设计。将于2025年8月到期的《药品供应链安全法案》(DSCSA)更为严格的实施期限,迫使资金雄厚的运营商进行序列化投资,而这些投资只有在具备相应条件的情况下才可行,从而赋予他们收取溢价的自由裁量权。基于GLP-1的体重管理疗法的快速增长、细胞和基因疗法的稳步发展以及直接面向患者(DTP)服务的扩张,进一步扩大了美国药品物流市场,要求运营商迅速提升其温控能力。同时,製造商正在开发现有药物的常温稳定版本,以降低不断上涨的运输成本。这减缓了非冷藏配送的相对成长,但为附加价值服务(VAS)供应商创造了新的包装和标籤业务。区域网络正在重组,中西部地区作为全国枢纽的份额不断扩大,而南部地区的运力扩张则缓解了沿海走廊的拥挤状况。
温控运输成本是常温运输的三到五倍,在已开发市场分销的治疗药物中,目前有80%需要在2-8°C的温度下储存,这进一步增加了低温运输的复杂性。 UPS采取了先发制人的行动,于2025年4月以16亿美元收购了Andlauer Healthcare Group,新增了170万平方英尺符合GDP认证的仓库空间,并扩展了其-80°C的冷冻库网路。生物製药需要更短的订单到交货週期,因此对高频补货路线的需求高于大宗货物运输。小型承运商难以资金筹措持续监控系统的资金,这些系统需接受FDA的偏差记录审核,加速了产业的整合。次市场低温运输设施的激增为营运商提供了地域上的柔软性,但也需要在额外的交接点进行库存调整,这进一步凸显了基于人工智慧的路线可视性的重要性。
美国食品药物管理局 (FDA) 强制要求处方药在 2025 年 8 月前实现全程单元级可追溯性,这使得美国药品物流市场分为两类:一类是具备序列化能力的供应商,另一类是权限有限的供应商。 TraceLink 的 B2N 网路在 90 天内处理了 600 万个 EPCIS 事件,但资料错误率高达 30%,这可能导致每日产品隔离,凸显了实施的复杂性。预计每件可售产品的初始系统成本为 0.06 美元,这促使第三方物流专家采用共享解决方案。将 DSCSA 合规性纳入附加价值服务(VAS) 包的供应商不仅可以获得固定费用,还能加深买家对数位生态系统的依赖,从而实现召回管理、缺货预防和契约製造监管。
由于2024年至2025年间WTI原油现货价格波动幅度高达23%,药品托运商面临燃油额外费用计算公式不稳定、落后于成本飙升数週的困境。温控卡车由于冷冻装置的运作,柴油消耗量增加了12%,加剧了风险。液化天然气和电动牵引车的试验前景可观,但续航里程的限制和充电网路的不足制约了它们在东西向跨大西洋航线上的应用。路线优化软体和多站点运输模式可以减少空驶里程,但产品完整性规则仍然限制了货物的整合。
儘管运输仍然是收入的基础,但美国医药物流市场正明显地向一体化解决方案转型。 2025年,运输收入占比为70.45%,但预计从2026年到2031年,附加价值服务将以4.75%的复合年增长率超越运输收入,这主要得益于客户对序列化、重新贴标和套件组装等服务以及货运需求的增加。公路货运的份额依然强劲,这主要得益于最后一公里配送和向乡村诊所的配送,而感测器和双隔间拖车的应用也有助于加强合规性。儘管空运成本较高,但它在细胞疗法和其他特殊用途货物的运输方面仍然占据着独特的地位,因为这些货物的运输不容延误。随着托运人越来越多地使用温控冷藏集装箱来运输从亚洲到美国的稳定药物原料药,海运业务正在扩张,这不仅符合ESG目标,还能在空运运力短缺时提供运力。
由于缺乏符合GDP标准的转运点,铁路运输仍受到限制。由于《药品分销安全法》(DSCSA)提高了可追溯性要求,仓储需求紧张。仓库正在转型为数位化序列化中心,以便在发货前检验二维资料矩阵码,而自动化计划(视觉系统扫描器和自动托盘运输车)正在减少合规性检查的延误。成长最快的是附加价值服务(VAS)领域,其中包括托盘重新配置、紧急客製化以及进出口差异的记录。
The United States Pharmaceutical Logistics Market was valued at USD 75.96 billion in 2025 and estimated to grow from USD 78.53 billion in 2026 to reach USD 92.67 billion by 2031, at a CAGR of 3.38% during the forecast period (2026-2031).

The United States pharmaceutical logistics market size projection underscores how compliance deadlines and biologics demand are reshaping cost structures and service design. A tightening Drug Supply Chain Security Act (DSCSA) timetable, expiring in August 2025, forces serialization investments that only well-capitalized providers can execute, granting them premium pricing latitude. Surging GLP-1 weight-management therapies, the steady rise of cell and gene treatments, and direct-to-patient (DTP) fulfillment further enlarge the United States pharmaceutical logistics market, pressing operators to expand temperature-controlled capacity at speed. Manufacturers are simultaneously formulating ambient-stable versions of existing drugs to curb rising freight costs, tempering the relative growth of non-cold-chain flows yet creating new packaging and labeling work for value-added service (VAS) providers. Regional network redesign is underway, with the Midwest gaining share as a national hub while capacity additions in the South ease congestion on coastal corridors.
Temperature-controlled transport costs three to five times more than ambient freight, and 80% of therapies shipped in developed markets now need 2°-8 °C custody, elevating cold-chain complexity. UPS moved early by paying USD 1.6 billion for Andlauer Healthcare Group in April 2025, adding 1.7 million ft2 of GDP-certified storage and extending its -80 °C freezer network. Biologics also shorten order-to-delivery cycles, driving demand for high-frequency replenishment lanes rather than bulk shipments. Smaller carriers struggle to finance the continuous monitoring systems the FDA now audits for excursion logs, accelerating consolidation. As cold-chain nodes multiply in secondary markets, operators gain geographic flexibility but must coordinate inventory at added hand-off points, intensifying the need for AI-driven route visibility.
The FDA requires full unit-level traceability on prescription medicines by August 2025, splitting the United States pharmaceutical logistics market between serialization-ready providers and those facing restricted access. Implementation complexity is evident in TraceLink's B2N network, which processed 6 million EPCIS events in 90 days yet logged a 30% data-error rate that could trigger daily product quarantines. Up-front system costs, estimated at USD 0.06 per saleable unit, invite pooling solutions run by third-party logistics specialists. Providers that embed DSCSA compliance into VAS packages not only lock in retainer fees but also deepen buyer dependence on their digital ecosystems for recall management, shortage mitigation, and contract manufacturing oversight.
WTI spot prices swung 23% in 2024-2025, leaving pharma carriers with unmatched fuel-surcharge formulas that lag cost spikes by weeks. Temperature-controlled trucks burn 12% more diesel to power reefers, amplifying exposure. While LNG and electric tractor pilots show promise, range limits and sparse charging networks curtail adoption on coast-to-coast lanes. Route-optimization software and multi-stop milk-run models reduce empty miles, but product-integrity rules still cap load consolidation.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Transportation still anchors revenue, yet the United States pharmaceutical logistics market shows a clear migration toward bundled solutions. In 2025, transportation delivered 70.45% of turnover, but value-added services are expected to outpace at a 4.75% CAGR (2026-2031) as clients seek serialization, relabeling, and kitting alongside freight. Road freight's share remains resilient due to final-mile and rural clinic deliveries, with sensors and dual-compartment trailers adding compliance. Air freight, while costly, preserves its niche for cell therapy and compassionate-use shipments that tolerate no delay. Ocean carriage gains as shippers divert stable formulation APIs to controlled-atmosphere reefers on Asia-to-US lanes, aligning with ESG goals and securing uplift during air-capacity crunches.
Rail remains marginal, hindered by limited GDP-certified hand-off nodes. Warehouse & storage demand tightens as DSCSA elevates traceability, turning depots into digital serialization hubs where 2D data-matrix codes are verified before release. This pushes automation projects-vision-system scanners and autonomous pallet movers-to squeeze latency out of compliance checks. The fastest growth occurs in VAS, including pallet reconfiguration, late-stage customization, and documentation for import-export variance.
The United States Pharmaceutical Logistics Market Report is Segmented by Service Type (Transportation, Warehousing & Storage, and Value-Added Services & Others), Mode of Operation (Cold-Chain Logistics and Non-Cold-Chain Logistics), Product Type (Prescription Drugs, Biologics & Biosimilars, Veterinary Medicine, and More), Region (Northeast, Midwest, South, and West). The Market Forecasts are Provided in Terms of Value (USD).