The CDMO Partner You Need.
Seamless Supply with True End-to-End Support
As pharma innovators, your CDMO partner must bring the expertise, scale, and regulatory strength to support your programs at every stage. With decades of experience across six technology platforms, a global network expansion spanning three continents, and hundreds of years of combined facility expertise, we deliver true end-to-end services across the complete drug lifecycle, from drug substance to drug product. Our integrated capabilities and expanded capacity enable consistent execution, supporting development, clinical supply, and large-scale commercial manufacturing with confidence.
(in 2025)
(in 2025)
(in 2025)
We understand what is at stake in your API program and bring decades of experience in development and manufacturing to ensure a reliable, high-quality drug substance supply that keeps your project progressing with confidence.
Our API development & manufacturing capabilities include:
Our broad spectrum of drug product capabilities spans from clinical development through commercialization across a wide range of dosage forms, including Oral Solid Dosage (OSD), Aseptic Fill and Finish sterile injectables, and Oral Peptide Delivery, covering multiple modalities, including highly potent compounds. With advanced packaging, labeling, and serialization capabilities, we deliver reliable, high-quality drug product supply to support your program at every stage.
Our Drug Product development & manufacturing capabilities include:
We are a global CDMO leader in pioneering specialized lipid-based products, supporting the development and manufacturing of nanomedicines with expertise in synthetic lipid process development, LNP formulation, scale-up, and large-scale manufacturing. Our high-quality lipid excipient building blocks, LNP starter kits, and cutting-edge technologies support your supply of lipid-based medicines, no matter the scale or phase of development.
Our Lipid Excipient and Nanomedicine capabilities include:
Managing multiple CDMOs across development stages and technologies increases coordination effort, risk, and timelines. CordenPharma integrates development and manufacturing of complex modalities across APIs, Drug Products and Packaging at all scales, coordinated through a global delivery and project management model.
What this means for you:
With fully-integrated cGMP facilities across Europe and North America, our small to large-scale manufacturing capacities and technologies provide the reliable outsourcing services you need, spanning your complete supply chain from early clinical-phase development to commercialization.
Our approach to every project begins with fostering a constant exchange between the applicable API, Drug Product and Lipid Excipient process development teams involved. Ongoing alignment with analytical, quality and compliance support allows for faster and more consistent results, regardless of where your project starts.
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