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AMRI offers specialized aseptic formulation development and manufacture of small batches for early-stage clinical trials.

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We advance the development of quality products such as extended release solid oral dosage forms and DEA controlled substances, as well as cGMP clinical supplies.

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We use GMP facilities to manufacture batches of development products that can be used for clinical trials to support the validation of the product concept and for the later approval process.

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Wide variety of dosage forms and flexible batch sizes. Contact us for more information.

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As a regular producer of pharmaceutical active ingredients, Pierre Fabre operate in full compliance with current Good Manufacturing Practices (GMP, ICHQ7A). We are also regularly inspected by EMA and FDA.

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Glatt's facilities and quality-assured processes are GMP compliant manufacturer of placebo and verum for clinical studies in lab and on a pilot scale. Our services include the manufacture of clinical test samples for all solid dosage forms that can be imp

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Softigel's seven cutting-edge facilities house a fully integrated PDS unit and covers all product life cycle phases from early development to commercial in the same plant, using equipment replication between non GMP and GMP.

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Summit Biosciences is a specialty pharmaceutical company focused on developing, manufacturing and commercializing generic and innovative nasal spray drug products.

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Pharmatis has been conceiving and developing various recipes, processes and drugs for many years. Pharmatis offers production of batches for clinical trials.

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With eight facilities in the US, EU, and Asia/Pacific region, and more than 50 depots covering 6 continents, Catalent Clinical Supply Services has a robust network built around flexible and integrated service offerings for pharmaceuticals in clinical tria

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The formulation scientists at Cook Pharmica have great experience in a variety of formulations and product presentations. For products that need the added stability of lyophilization, the required lyophilization cycles can be optimized through the use of a LyoStar II™ development lyophilizer.

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Additionally, Curida offers following services across all technologies: Manufacturing of investigational products for clinical studies

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Delpharm propose its knowledge and experience to manufacture licensed products, generics, OTC products, dietary supplements, veterinary products, medical devices, highly active and injectable products.

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Neuland provides drug development support by supplying of clinical trial material.

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Why involving various suppliers when one partner is able to meet your clinical supply material needs Our business is to develop and manage your clinical supply materials, from design to delivery. We bring your API to clinics within a typical timeframe o

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Our development facilities allow us to cater for a range of clinical trials from preclinical to smaller Phase III trials. For very large clinical batches we can arrange manufacture in one of our commercial manufacturing units. So whatever stage you’re at,

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Aizant's scientists use Quality-By-Design (QbD) tools at all stages of formulation development. Design of experiments (DOE) along with risk assessment strategies allows us to design our experimental plan.

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Aizant's scientists use Quality-By-Design (QbD) tools at all stages of formulation development. Design of experiments (DOE) along with risk assessment strategies allows us to design our experimental plan.

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Siegfried offers a broad base of know-how in complex oral and sterile formulations of drug products available for custom development and manufacturing (CDMO), and licensing.

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FAMAR Technical R&D offers the full range of services for Pharmaceuticals (Rx & OTC) across all dosage forms and Dermocosmetics and Cosmetics (Healthcare & Hygienic). Famar has 4 sites in three countries – France, Greece and Spain.

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Servier brings 60 years of experience in process development, intermediates, APIs and high-potency APIs. Our full cGMP / FDAapproved chemistry network includes R&D, production and supply chain expertise with full regulatory support. Servier CDMO’s teams are able to follow your projects from

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We perform formulation assessment, early stage proof of concept, formulation selection, design of experiments, pre formulation, release profile determination, formulation strategy, process development, optimization and technology development.

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We perform formulation assessment, early stage proof of concept, formulation selection, design of experiments, pre formulation, release profile determination, formulation strategy, process development, optimization and technology development.

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Galenix can produce very large batches of blinded treatments in accordance with a very important range of clinical supplies requirements in short delays, with a trained team of operators and fully automated or semi-automated equipments.

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By delivering integrated pharmaceutical development services, we ensure a seamless transition from pre-formulation, to formulation development, to the supply of clinical trial materials.