Source: CNN
In a decisive move to reinvigorate domestic pharmaceutical manufacturing, President Donald Trump signed a new executive order designed to bring prescription drug production back to American soil. The order, announced in May 2025, comes at a pivotal time—just weeks ahead of proposed tariffs on imported pharmaceuticals, which could reshape the global drug supply chain and significantly impact the cost and availability of medications in the U.S.
The initiative is part of Trump’s broader "America First" economic policy, with an added sense of urgency following global supply chain disruptions seen during the COVID-19 pandemic and escalating geopolitical tensions with China and Europe.
The order directs the U.S. Food and Drug Administration (FDA) to accelerate the approval process for new pharmaceutical manufacturing plants by:
This measure is aimed at reducing red tape and shortening the current 12- to 18-month approval timeline for pharmaceutical production facilities.
The U.S. pharmaceutical manufacturing base has significantly declined over the last three decades. According to the FDA, more than 80% of the active pharmaceutical ingredients (APIs) used in American medications are now produced overseas—primarily in China, India, and Europe—due to cheaper labor, raw materials, and operational costs.
In 2023, the U.S. imported approximately $203 billion worth of pharmaceutical products, according to data from consulting firm Ernst & Young (EY). Of that, 73% originated from European nations like Ireland, Germany, and Switzerland, which have become central hubs for high-value pharmaceutical production.
As part of his broader trade policy, Trump is proposing a new wave of pharmaceutical import tariffs, which could go into effect later in 2025. These tariffs are expected to target nations heavily exporting drugs to the U.S., including key partners in Europe and Asia.
The goal: to create a pricing advantage for domestically produced drugs, encourage pharmaceutical companies to build and expand U.S.-based facilities, and reduce reliance on foreign supply chains that have proven vulnerable during global crises.
A report from GlobalData, a healthcare analytics firm, notes that reshoring drug production could strengthen the national drug supply chain, lowering the risk of shortages and improving national security in healthcare.
However, this strategy does come with trade-offs. Domestic production is likely to raise operating costs, which could lead to higher drug prices for consumers in the short to medium term.
The Generic Pharmaceutical Association (GPhA) expressed cautious support for the initiative but emphasized the need for government subsidies, tax credits, and public-private partnerships to make domestic manufacturing economically viable.
Industry leaders are responding with mixed reactions. While some view the order as a bold and necessary step, others warn of unintended consequences.
“We applaud the administration’s focus on securing the drug supply chain, but the transition needs to be carefully managed to avoid price shocks,” said Dr. Laura McKinley, spokesperson for the American Pharmacists Association.
Meanwhile, pharmaceutical giants like Pfizer and Amgen have begun exploring expansions of their U.S. facilities, with new investments totaling over $2.5 billion announced in recent months. Smaller contract manufacturing organizations (CMOs) are also gearing up to bid for federal incentives under the new policy framework.
Trump’s executive order marks a turning point in how the U.S. views its pharmaceutical future. By shifting focus back to domestic production, the administration is prioritizing supply chain resilience, national security, and economic independence in the healthcare sector.
Whether this shift can be achieved without significantly increasing drug costs remains to be seen. But one thing is certain: The global pharmaceutical map is about to change, and the U.S. is determined to be back at the center of it.