Compare drug product CDMOs for formulation development, solid oral dosage, sterile injectables, and specialty dosage forms. Filter by dosage type, scale, and certifications.
1364 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.
Spain
TRADICHEM is a Spanish company that develops innovative, science-based ingredients for the pharmaceutical and nutraceutical industries, with 15 proprietary ingredients backed by clinical studies, present in 2,500+ final products across 52 countries. Its subsidiary TIS Pharma operates EU GMP-certified facilities providing pharmaceutical API compaction and granulation services using their patented HIPERING technology. TRADICHEM also operates MarenostrumTech for botanical extract production. While TIS Pharma provides contract processing services (compaction/granulation of APIs), the company is primarily an ingredients supplier rather than a full CDMO.
Italy
Truffini & Reggè Farmaceutici Srl is an Italian company founded in 1917 that specializes in developing and producing food supplements, medical foods, and medical devices exclusively for third parties (private label). Certified ISO 9001, ISO 13485, ISO 22000, and FDA CFR 21 Part 111 for dietary supplements. They manufacture supplements and nutraceuticals, NOT pharmaceutical drugs.
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India
UNIPRO Sp. z o.o. is a Polish company (near Krakow) specializing in private label contract manufacturing of food supplements, functional food, and sport nutrition products. They serve pharmaceutical, food retail, veterinary, drugstore, and sport nutrition markets. They produce capsules, tablets, bars, protein products, and powders but these are dietary supplements and functional foods, NOT pharmaceutical drugs. Despite being listed with India as headquarters, they are a Polish entity.