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Bioindustria L.I.M specializes in large and small volume injectables with terminal sterilization or with aseptic process.

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As regards parenteral drugs, Polpharma offers contract production services with respect to liquid dosage forms using the BFS (blow-fill-seal) technology, including injectables in polyethylene containers.

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Quotient Sciences has responded to the challenges associated with the manufacturing of today’s high-potency drug products by ensuring our facilities are capable of handling compounds with a maximum performance-based level of exposure classification.

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Eurofins CDMO offers integrated development services through the entire drug product life cycle, from highly potent active pharmaceutical ingredients (HPAPI) forward.

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ScinoPharm provides one-stop-shop service for our existing API customers. The company also adopts Double A (API+ANDA) business model to team up with Pharma companies' to apply for ANDA in US/EU and export final drug products globally.

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Development, manufacture and control of generic pharmaceutical specialties, both for Neuraxpharm and other laboratories, performed at Lesvi facilities in Sant Joan Despí (Barcelona), Spain

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BIOPHARMA an FDA approved CMO for betalactam antibiotics finished products, with a wide, global and skilled experience in contract manufacturing produces various oral and injectable products.

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BIOPHARMA started its activities in 1995 and today is a leading ß -lactams antibiotics manufacturer, with a wide, global and skilled experience in contract manufacturing. The facility, located in Rome’s industrial area of Santa Palomba, is approved by the Italian Authority for the oral and

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Today Injectalia, after some important investments in new technologies, in segregated different buildings, mainly manufactures pharmaceutical products under different forms: Pre-filled syringes

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Carbogen Amcis SAS located in Riom, France, focuses on the development and manufacturing of formulation dosages, aseptic filling, and lyophilization of small-molecule APIs, highly-potent APIs and biologics.

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Softigel is specialized in Softgel technologies and offer access to other delivery systems such as sterile liquids, injectables, prefilled syringes, creams, ointments, gels, powders, tablets and hard gel capsules.

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We manufacture, supply and distribute commercial formulations from our facilities in UK and India for Oral Solids and Lexington, USA for Sterile Injectables.

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Steril-Gene has 4 major state-of-the-art manufacturing facilities for hormone formulation for softgelatin capsules, tablets, potent tablets/capsules, liquid injection in ampoules, vials, lyophilized vials and general oral solid dosages

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From IND applications through commercial scale production, we provide formulation and compounding, fill-finish, and optional lyophilization services for a wide variety of liquid injectables.

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Curida’s core competency is in state-of-the-art manufacturing of sterile liquid pharmaceuticals based on nunit-dose Blow-Fill-Seal (BFS) technology, ensuring a high quality, fast and robust process with minimal human intervention

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Our team combines expertise in drug formulation development for generic applications or new chemical entities with an understanding of commercial pharmaceutical manufacturing processes for long acting forms, sterile injectables and hormonal tablets.

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Flagship biotech has capability to manufacture high quality Solid & Liquid Dosage Form, LVP, SVP, Speciality Injectables, Powder for Injections, Inhalers, Ointments and Creams etc.

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Legacy Pharmaceutical offers a wide range of possibilities for production and aseptic filling of liquid parenteral dose forms, at multiple filling facilities. Legacy Pharmaceutical is also equipped for thermal final sterilization.

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Panpharma offers a range of narcotics (“controlled drugs”) and ensures complete traceability of products from the raw material to the finished product and end hospital.

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The manufacturing in compliance with Romanian law no 95/2006 regarding medicines for human use. Valid Manufacturing Authorization, in full compliance with GMP issued by the National Medicine and Medical Devices Agency.

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Brooks Laboratories a WHO GMP & ISO 9001:2008 certified company is in the business of pharmaceuticals and is in contract manufacturing, marketing and exports.