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Quotient Sciences' innovative approach to formulation development integrates drug product development with clinical evaluation, combined with our experience with over 1,000 molecules at all stages of drug development.

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Skyepharma's experts can apply extensive range of proprietary technologies for modified release, pulsed release, timed release to solve technological challenges, to provide patient benefits & to offer additional proprietary protection to the product.

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Our formulation optimization services include Drug characterization for physical and chemical properties, Solubility and solution stability studies, including pH profiles and Excipient/compound compatibility studies

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Medichem offers a wide range of contract services, may that be manufacturing of APIs (including HPAPIs) or manufacturing and packaging of the finished dosage form, testing and release services.

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

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Magle strives to excel in the technical and medical development of polysaccharide products for healthcare. Our core knowledge is rooted in the design and development of in-vivo Degradable Starch Microspheres (DSM).

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Ascent offer end to end pharmaceutical formulation development services of Immediate Release tablets ranging from early phase development to clinical supplies for new chemical entities, generics and life cycle extension products.

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Pierre Fabre experts use a maximum number of natural ingredients in the products and design biodegradable formulas for rinse-off products. The following products are created in this way: emulsions, foaming products, lotions, sticks, powders, soaps, oils

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JGL's evergreen technologies are traditional pharmaceutical forms that include solid oral forms (tablets, capsules and granules), non-sterile solutions (like syrups and drops), and semisolid forms (ointments, creams and gels).

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Gentec Pharmaceutical Group offers API, intermediates and HPAPIs developments and manufacture in our plants, Duke Chem and Pharmanoid, under contract manufacturing.

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Biophore, an established pharmaceutical company, is engaged in the development and manufacturing of niche pharmaceutical products for the generic industry. Biophore has emerged as a trusted partner in the generic industry across US, Europe and other regulated markets.

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Eurofins Contract Development & Manufacturing Organization provides integrated, end-to-end drug development solutions supporting clients from the earliest phases of API research and development through finished products.

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Eurofins CDMO has considerable experience with process development, successfully introducing hundreds of chemical steps to cGMP scale up and advancing several API’s to commercialization.

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Recro provides robust formulation development services that support the development of a variety of pharmaceutical products.

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ParticleMax™ is a spray drying particle engineering technology was developed to deliver dry powder biologics and can produce uniform mixtures of drugs and excipients and can be used to co-formulate multiple APIs in the same particle at a fixed ratio.

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The Regulatory Department in Orofino Pharmaceuticals Group has extensive experience in dealing with regulatory transfers and is able to assist in the regulatory process of managing dossier updates and transfer submissions.

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Over the past 25 years, Unither has acquired deep expertise in drug product development and manufacturing based on its different technologies (Blow-Fill-Seal, Powder/Liquid stick packs, orodispersible tablets, syrups, suspensions, solutions, …)