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.

  • Multiple cGMP Facilities across Europe and the United States
  • Track record of scientific, operational, R&D and sales expertise
  • State-of-the-art facilities with a wide breadth of capabilities

Bergamo, IT

Bergamo, IT
Facility Capabilities
  • cGMP custom synthesis from lab to multi-tonne scale
  • Multi-step API process development, manufacturing and analytical development
  • Industrialization from feasibility to commercial scale
  • Regulatory filing in the US, EU and Japan
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Boulder, US

Boulder, Colorado, USA
Facility Capabilities
  • cGMP development & manufacturing of intermediates and chemically synthesized APIs
  • Synthetic peptides, highly potent cytotoxic and non-cytotoxic APIs
  • Large-scale peptide production
  • Manufacture of high volume small molecule APIs
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Brussels, BE

Brussels, BE
Facility Capabilities
  • Solid-phase peptide synthesis (SPPS)
  • Liquid-phase peptide synthesis (LPPS)
  • Hybrid strategies (SPPS-LPPS)
  • Complex peptides and peptidomimetics
  • Peptide-conjugations (PEGs, proteins, lipids, carbohydrates)
  • Cyclic peptides & peptides with multiple disulfide bridges
  • Short peptides (10-12 residues), often with no HPLC purification
  • Arginine-rich peptides
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Caponago, IT

Caponago (Monza & Brianza), Italy
Facility Capabilities
  • Formulation & packaging of parenteral dosage forms
  • Sterile emulsion technology
  • Pre-filled syringes
  • Clinical trial services
  • Formulation development
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Chenôve, FR

Chenôve, France
Facility Capabilities
  • cGMP custom synthesis from kilolab to multi tonnes scale
  • Multi-step API process development and manufacturing
  • Industrialisation from feasibility to commercial scale
  • Production of bulk pre-mixed drug products 
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Latina, IT

Sermoneta, Italy

Facility Capabilities

  • cGMP manufacturing of oral and sterile liquid dosage forms for cephalosporins, penicillins and cytotoxics
  • Manufacturer of sterile cephalosporin and penicillin drug substances
  • Full range of development and packaging services
  • Fully integrated infrastructure
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Liestal, CH

Liestal, Switzerland

Facility Capabilities

  • Route scouting & process development for APIs, intermediates and chiral building blocks
  • Development and cGMP manufacturing of APIs and other chemically synthesised materials
  • Lipids, peptides, carbohydrates, AADs and pseudoproline dipeptides
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Plankstadt, DE

Plankstadt, Germany
Facility Capabilities
  • Manufacturer of oral solid dosage forms
  • Extensive primary & secondary packaging capacity
  • Special expertise in formulating highly potent products
  • Full range of services including formulation and process development, manufacturing of investigational medicinal products & pharma-logistics
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Frankfurt, Germany
CordenBioChem Capabilities
  • Contract Development & Manufacturing Organization (CDMO) of microbial fermentation, technical enzymes and the application of biocatalysis for the synthesis of intermediates and APIs
  • Process development and characterization from initial pilot scale (3 x 15L) to industrial large-scale up to 120m³-scale, including process validation
  • Capability to handle a wide range of organisms (e.g. fungi, E.coli, Pichia, Bacillus, other yeast) as non-GMO organisms and GMO-organisms up to BSL 1
  • Dedicated cell bank preparation facility and maintenance with redundant equipment and controls
  • On-site anaerobic and aerobic waste treatment
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