Thermo Fisher Scientific’s state-of-the-art contract API development and manufacturing facility in Cork supports our customers in bringing medicines to patients through the relentless application of science in process and analytical development.
We take chemistry from laboratory-scale development through to large-scale commercial supply, made possible by our driven and dedicated employees — a team of 500+ highly skilled chemists, engineers, analysts, operators, and crafts personnel.
Our facility meets the most stringent production, compliance, safety, and environmental standards. We take pride in our mission to enable our customers to make the world healthier, cleaner, and safer through API development and manufacturing.
This site provides flexible and multipurpose facilities, including these onsite offerings:
Specialized capabilities:
Learn more about the specific equipment and capabilities at this site by downloading our fact sheet.
Brochure
Small molecule API solution: Taking a big picture approach
With competitive options for API outsourcing in all geographical regions, it can be difficult to choose the right partner for your project, regardless of its complexity. Thermo Fisher Scientific...
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Bioavailability enhancement technologies for poorly soluble molecules
It’s estimated that about 40% of drugs with market approval and nearly 90% of molecules in the discovery pipeline are poorly soluble. This can impede drug absorption, leading to reduced bioavailability and compromised therapeutic efficacy. Explore how Thermo Fisher Scientific’s Quadrant 2 platform leverages AI/ML tools to identify solubility enhancement technologies.
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Route Scouting for a cost-effective process development
In this webinar, experts from across Thermo Fisher Scientific’s global network will describe key benefits of route scouting and polymorph screening at early stages of clinical trials to ensure scalability for early clinical supplies to commercial manufacturing.
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Advancing drug development using in silico modeling
This report provides a framework for that understanding by outlining some of the processes that stand to gain the most from computational modeling and identifying the in silico capabilities that can be used to accelerate and de-risk each phase of development.
View whitepaperCase study
Midsize pharma company stabilizes API - Accelerates time to clinic from three months to three weeks
A midsize pharma company wanted to progress its therapy from early development to late-phase clinical trial stage, but needed a CDMO partner to provide support in formulation analysis so that it could stabilize its product and successfully reach its clinical studies milestones.
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Mastering complex small molecule APIs and formulations
Complex small molecule APIs are characterized by their intricate structures, higher molecular weights, and sophisticated delivery requirements, which pose unique challenges in their formulation and manufacturing processes.
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