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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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We have extensive experience in formulation development in solving complex formulation challenges. Our experts will advise you on the best solution to optimise drug delivery for the benefit to the patients.

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AMRI's scientists provide support and direction to design robust formulations for preclinical and clinical use.

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The formulation development center at Ascent offers physico-chemical characterization that includes pH- solubility profile, Solubility in various aqueous and non-aqueous vehicles, pH- stability profile, Melting point, Hygroscopicity, Polymorph characteriz

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Pierre Fabre Group offers pharmaceutical and non-pharmaceutical subcontracting activities (CDMO) which combine a high level of quality, skill and performance. Our teams of specialists support you in the development and industrialization of your products.

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Our services under Galenic development include Formulation studies, Studies for excipient compatibility, Establishing quali/quantitative fomulae, Design of manufacturing methods, Establishing in-process controls, Transfer of technology to the customer

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We use our platform technologies to develop, scale up & commercialize products for our clients for various markets. We provide complete solutions for the partner’s product needs right from prototype development, industrial scale up to Commercial Supplies.

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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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Recro provides solutions for complex formulations with robust formulation development services to support drug product development. We advance the development of quality products such as ER oral solids, DEA controlled substances, cGMP clinical supplies.

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Vectura (GMP Compliant) is able to apply our technologies to product development programmes through all stages of pharmaceutical and product development, including pivotal clinical trials and technical transfer to commercial production.

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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)

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With over 10 years of experience in the fast supply of clinical trials batches, Carbogen Amcis SAS offers comprehensive services in formulation and for aseptic drug products for a wide range of products, including oncology and metabolic disorders therapeutics.

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Pierre Fabre Group offers pharmaceutical and non-pharmaceutical subcontracting activities (CDMO) which combine a high level of quality, skill and performance. Our teams of specialists support you in the development and industrialization of your products.

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The development of solid dosage forms is our specialty, with focus on complex formulations and vast expertise for multiparticulate systems. Our development and manufacturing centers with FDA and EU-GMP certification are well equipped for all your requirem

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We focus on our customer needs and support the product lifecycle covering phases starting from development, technology transfer, regulatory phase, market launch and lifecycle product upgrades.

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Catalent has 20 R&D teams with development and formulation expertise to help solve some of the most complex bioavailability challenges.

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Aizant's formulation laboratories are fully equipped for development of any product from NCEs to generics including specialty products.

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Dedicated team of highly qualified team of scientists, pharmacists and engineers having in-depth knowledge and vast experience of project management as well as Formulation and Development (FnD)

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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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Eurofins CDMO offers expert capabilities for the development, preparation & characterization of a variety of microbial, mammalian & insect cell banks. We offer the complete portfolio of cell banking services, with the manufacture of cell banks under cGMP.

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We have 30 years of experience in the development of products using our oral drug delivery technologies and expertise. We provide a comprehensive range of development services from feasibility studies to full formulation development and scale-up of comple

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PSR has necessary expertise & access to advanced technologies to develop the formulation and also, through the use of targeted analytics, supply the client with the relevant information needed to aid in the correct selection of formulation/drug delivery system to meet the clients requirements.

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In the field of pharmaceutical drugs, IDT focuses on sterile, injectable, bioengineered finished products. Here again, IDT Biologika handles the entire process chain, from development to ready-for-sale packaging of pharmaceutical products.