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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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Our technical team has considerable experience in the process development & optimization of complex formulations to ensure the critical process parameters are properly controlled, and that the processes are cost-effective and robust at multiple scales.

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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, Contract Services offered for FDF Oral Solid Dosage Forms.

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

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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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We support the production process/technology transfers and expansion of current manufacturing capabilities including investments, the implementation of quality standards, practise and training etc.

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Different Departments of Production, QC, R&D at Temad Co. have gained invaluable experiences & are in a position to transfer technology to other companies. In addition, We are able to transfer technology of foreign sources to interested domestic companies

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We support your API development & manufacturing requirements. Our CDMO Services include technology transfer, process development, analytical methods development, synthesis of impurities & standards, potential genotoxic impurities evaluation etc

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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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Athena's EU GMP approved facility in India can handle a vast majority of dosage forms like bilayer tablets, capsules, sachets, orally disintegrating tablets and conventional dosage forms for various clients in advanced and pharmerging markets.

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Biophore, is engaged in the development & manufacture of niche pharmaceutical products & modified oral solid dosage forms (Tablets, Capsules). It has emerged as a trusted partner in the generic industry across US, EU & other regulated markets.

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Eurofins CDMO provides integrated, end-to-end development and manufacturing services for Drug Substance/API and Drug Product manufacturing for biologics and small molecules.

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Eurofins CDMO has a high degree of expertise process development, successfully introducing hundreds of chemical steps to cGMP scale up and advancing several APIs from route scouting through to commercialization.

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

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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.