We are bringing together the facilities of leading pharmaceutical and biotechnology companies to provide you with a full suite of services spanning the entire pharmaceutical product continuum.
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Multiple cGMP Facilities across Europe and the United States
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Track record of scientific, operational, R&D and sales expertise
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State-of-the-art facilities with a wide breadth of capabilities
Bergamo, IT
Facility Capabilities
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cGMP custom synthesis from lab to multi-tonne scale
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Multi-step API process development, manufacturing and analytical development
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Industrialization from feasibility to commercial scale
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Regulatory filing in the US, EU and Japan
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Caponago (Monza & Brianza), Italy
Facility Capabilities
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Formulation & packaging of parenteral dosage forms
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Sterile emulsion technology
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Pre-filled syringes
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Clinical trial services
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Formulation development
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Chenôve, France
Facility Capabilities
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cGMP custom synthesis from kilolab to multi tonnes scale
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Multi-step API process development and manufacturing
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Industrialisation from feasibility to commercial scale
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Production of bulk pre-mixed drug products
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Boulder, Colorado, USA
Facility Capabilities
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cGMP development & manufacturing of intermediates and chemically synthesized APIs
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Synthetic peptides, highly potent cytotoxic and non-cytotoxic APIs
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Large-scale peptide production
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Manufacture of high volume small molecule APIs
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Cork, Ireland
Facility Capabilities
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Development and production of controlled substances
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Development of small molecule APIs and advanced intermediates
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Expertise in regulatory customer support
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Sermoneta, Italy
Facility Capabilities
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cGMP manufacturing of oral and sterile liquid dosage forms for cephalosporins, penicillins and cytotoxics
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Manufacturer of sterile cephalosporin and penicillin drug substances
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Full range of development and packaging services
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Fully integrated infrastructure
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Plankstadt, Germany
Facility Capabilities
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cGMP manufacturer of solid dosage forms
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Primary and secondary packaging capacity
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Highly potent product formulation
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API purification, formulation development, clinical trial supply and pharma-logistics
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Liestal, Switzerland
Facility Capabilities
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Route scouting & process development for APIs, intermediates and chiral building blocks
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Development and cGMP manufacturing of APIs and other chemically synthesised materials
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Lipids, peptides, carbohydrates, AADs and pseudoproline dipeptides
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