AHA Statement to House Energy & Commerce Subcommittee on Health Hearing for June 11, 2025

Statement

of the

American Hospital Association

for the

Committee on Energy and Commerce 

Health Subcommittee

of the

U.S. House of Representatives

“Made in America: Strengthening Domestic Manufacturing and the Health Care Supply Chain”

June 11, 2025

On behalf of our nearly 5,000 member hospitals and health systems and other health care organizations, our clinician partners — including more than 270,000 affiliated physicians, 2 million nurses and other caregivers — the American Hospital Association (AHA) appreciates the opportunity to submit this statement for the record to the Committee on Energy and Commerce Health Subcommittee hearing “Made in America: Strengthening Domestic Manufacturing and the Health Care Supply Chain.”

The AHA believes it is necessary to strengthen the domestic supply chain for essential pharmaceutical and other medical products and recognizes the value of reducing reliance on international sources. We are also aware that achieving this goal will require significant time due to the logistical complexity and resources involved in reorienting medical and pharmaceutical supply chains.

Each day in America’s hospitals and health systems, patients receive safe and effective care from provider teams using a wide array of pharmaceuticals and medical devices. Patients’ lives depend on the ready availability of drugs and devices to respond to emergent conditions like heart attacks and infections, and other critical illnesses like cancer and organ failure. The medical supply chains for pharmaceutical products and other medical devices are highly complex, requiring hospitals to draw on domestic and international sources. These supply chains are prone to significant disruption from a wide range of factors, including transportation interruptions, natural disasters, raw materials shortages and production breakdowns.

Despite ongoing efforts to bolster the domestic supply chain, international sources still supply a significant proportion of essential medical goods. For example, nearly 70% of medical devices marketed in the U.S. are manufactured exclusively overseas.¹ In 2024 alone, the U.S. imported over $75 billion in medical devices and supplies, according to AHA analysis of Census Bureau data. These imports include many low-margin, high-use essentials for hospital settings that are necessary for patient care. Some of these devices are single-use, designed to protect patients from infection, such as single-use blood pressure cuffs, stethoscope covers and sterile drapes. Others are small devices used ubiquitously in hospitals, such as anesthesia instruments, cautery pencils, needles, syringes and pulse oximeters. The low-margin nature of these products makes them difficult to produce within the U.S. At the same time, disruption in the availability of these devices would curtail hospitals’ ability to perform life-saving surgeries and keep patients safe from contagion, as well as hinder providers’ ability to effectively diagnose, monitor and treat patients.

Many pharmaceuticals are also sourced from overseas. For example, U.S. providers import many cancer and cardiovascular medications, immunosuppressives, antibiotics and combination antibiotics. For many patients, even a temporary disruption in their access to these needed medications could put them at significant risk of harm, including death. Carefully planned chemotherapy treatments and antibiotic schedules are essential to giving patients the best chance of overcoming their diseases. Similarly, the provision of necessary cardiovascular medications must be continuous to preserve their cardiovascular health.

As of the first quarter of 2025, there are 270 drugs on the active shortage list. A recent Government Accountability Office analysis found that the duration of drug shortages has increased, with nearly 60% of drug shortages lasting two or more years in 2024, compared to only one-third of shortages lasting that long in 2019.² In addition to finished pharmaceutical products, the U.S. sources many raw ingredients internationally for pharmaceuticals. These raw ingredients are commonly known as active pharmaceutical ingredients (APIs) and are the most important components of any pharmaceutical manufacturer’s supply chain. The U.S. gets nearly 30% of its APIs from China, and according to a 2023 Department of Health and Human Services estimate, over 90% of generic sterile injectable drugs — including many chemotherapy treatments and antibiotics — depend on APIs from either India or China. ³ While these statistics are an indicator of the importance of reshoring to protect America’s interests and strengthen the pharmaceutical and medical device supply chains, reshoring cannot, on its own, provide the supply chain stability needed to ensure unrestricted access to necessary drugs and devices for patient care. Included in the 270 active drug shortages are the lingering shortages of intravenous (IV) fluids stemming from the impacts of Hurricane Helene on a large North Carolina production facility in 2024.⁴ Despite that facility being located on American soil, it was not impervious to supply chain disruptions. While AHA is supportive of efforts to onshore and reshore pharmaceutical and medical device supply chains, domestic disruptions highlight the need for a diverse supply chain that includes international sourcing.

To that end, a critical step in protecting America’s pharmaceutical and medical supply chains is understanding vulnerabilities from the beginning of production to the moment a drug is administered to a patient or a device is used to deliver care. Supply chain vulnerabilities often only become apparent when the chain has been broken, as in the case of the IV fluid shortage that resulted from Hurricane Helene. Proactively mapping and assessing the pharmaceutical supply chain, as well as supply chains for other medical devices and equipment, is an important step to improving resiliency in U.S. supply chains and protecting patients’ access to care.

The AHA recently expressed support for S. 1784, the Mapping America’s Pharmaceutical Supply (MAPS) Act. The bill would codify a recent executive order from the administration to secure essential medicine supply chains.⁵ Additionally, it would require the Department of Health and Human Services to perform a comprehensive risk assessment of the entire U.S. pharmaceutical supply chain. The MAPS Act is an effective step toward strengthening the U.S. pharmaceutical and medical device supply chains. The AHA encourages the House of Representatives to take up similar legislation and look for more opportunities to encourage both onshoring and diversity in the supply chain to ensure health care resilience and protect U.S. national security.

Strengthening supply chains for essential pharmaceutical and other medical products is necessary, and the AHA recognizes the value of reducing reliance on international sources. Achieving this goal will require significant time and resources, given the complexity of medical and pharmaceutical supply chains, and the importance of supply chain diversity, in addition to the reshoring goal, should not be underestimated. AHA appreciates the committee’s attention to this topic and looks forward to further collaboration in the future.

⁴ https://www.ashp.org/drug-shortages/shortage-resources/drug-shortages-statistics

⁵ https://www.rickscott.senate.gov/2025/5/sen-rick-scott-colleagues-introduce-the-maps-act-to-boost-u-s-medicine-supply-chain-curb-dependence-on-communist-china