Compare drug product CDMOs for formulation development, solid oral dosage, sterile injectables, and specialty dosage forms. Filter by dosage type, scale, and certifications.
1365 companies listed
Drug product manufacturing transforms active pharmaceutical ingredients into the finished dosage forms patients use. This includes solid oral dosage (tablets, capsules), sterile injectables (vials, pre-filled syringes), semi-solids (creams, gels), and specialty forms (transdermal patches, inhalers, implants).
Formulation development is where science meets engineering. A CDMO's formulation team determines bioavailability, stability, and manufacturability. For poorly soluble compounds, techniques like spray drying, hot melt extrusion, and nano-milling can be the difference between a viable product and a failed program. Ask for specific experience with your compound class.
What scale do you need? Clinical-phase drug product often runs in batches of 5,000-50,000 units. Commercial scale might mean millions of units per month. Few CDMOs cover the full range efficiently. Match your current and projected volumes to a CDMO with the right equipment and batch size flexibility.
Italy
F.I.S. (Fabbrica Italiana Sintetici) is a privately owned Italian CDMO operating since 1957, specializing in the development and production of APIs and cGMP intermediates for the global pharmaceutical industry. The company offers contract development and manufacturing services including HPAPI production up to OEB3 containment from multiple production plants.
Switzerland
FRIKE Pharma AG is a Swiss pharmaceutical contract manufacturer (CMO) providing GMP-compliant contract manufacturing, filling, and packaging services for pharmaceutical products. The company specializes in liquid, semi-solid, and solid dosage forms including pump sprays, suppositories, lotions, ointments, and tinctures.
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