Our strategically located, FDA-inspected facilities across the U.S. help ensure scalable, phase-appropriate manufacturing solutions—from early development through first-in-human trials to commercial supply.
These sites are designed to reduce risk, speed transitions, and help keep your program moving—no matter the external pressures.
You gain supply chain assurance and flexibility through supplier diversification, strategic sourcing, foreign trade zones, and tailored logistics planning. Our teams work with you to develop continuity strategies that align with your business and regulatory needs.
Learn more about our
pharma supply chain solutions.
We currently operate four active FTZs at:
High Point, North Carolina
Cincinnati, Ohio
Manatí, Puerto Rico
Florence East, SC
Key advantages include:
We’re planning additional zones across the U.S. by 2026 to expand these benefits even further.
This policy is supported by cross-functional teams and harmonized processes. With built-in checkpoints for quality and performance, you gain a smoother path from development through launch—whether staying within the U.S. or transferring from global sites.
We offer extended terms agreements tailored to the needs of clinical programs, helping you manage resources during early development. Typical agreements range from 6 to 12 months, with options for further extension based on project milestones.
Thermo Fisher is investing $2 billion over the next four years to expand innovation, infrastructure, and capacity across our U.S. network:
“Thermo Fisher’s commitment to U.S. manufacturing reflects our confidence that America will continue to lead the world in science and innovation. By expanding our U.S. operations, we ensure that life-saving medicines and therapies will continue to be developed and produced in America for decades to come.”
— Marc N. Casper, Chairman, President, and CEO, Thermo Fisher Scientific (April 24, 2025)
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