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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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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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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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Softigel provides clients with access to formulation development, process development, CTM manufacturing, and scale-up services for a range of softgel types. From Phase I scale, scale-up and registration, through to large scale commercial production.

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We support the product lifecycle covering phases starting from development, technology transfer, regulatory phase, market launch and lifecycle product upgrades. We also provide scale-up testing, process optimization, process validation etc.

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The Formulation R & D Capability includes Design and development of new dosage forms, Pre formulation studies, Lab / pilot scale studies, Process optimization/validation studies, Stability studies as per ICH guidance, Technology transfer of new products.

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Ropack Pharma Solutions offers formulation development expertise for products at all stages. From early-stage prototype development, formulation selection, formulation optimization and release profile definition to late-stage formulation troubleshooting and lifecycle management formulations.

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Legacy Pharmaceutical supports you with process development, process validation & validation of analytical methods, commercial production, & sales of your products. Perfect planning and sustainable documentation result in successful product transfer.

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Our finished dosage form development team has successfully created numerous control release and extended release formulations, successfully ensuring afterward rapid scale up to full production.

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Progenerics Pharma is focused on developing high quality affordable generic products for global markets. Facilities are capable of developing all dosage forms like General Solids and injectables, Oncology Solids and Injectables including Lyophilized products, Creams & Ointments, Hormones and

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Flagship biotech had established A state-of-art Research and Development Centre (R&D) at Mumbai - focused towards developing new products, improving existing products as well as drug delivery systems and expanding product applications.

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SUSHEN Medicamentos (SUSHEN), is a global company of end-to-end pharmaceutical services with focus on drug delivery research and product development. SUSHEN’s expertise can bring a complex formulation project in to clinical and bioequivalence with superior quality, innovative solution.

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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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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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Sofarimex is the leader manufacturing company of pharmaceutical products in Portugal. This factory has a large productive flexibility, producing several pharmaceutical forms like solids, liquids, semi-solids & sterile products.

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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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Our development activities include Analytical Method Development & Validation, Process Development & Validation. Scaling, Pilot batches, batches for clinical trials, Production of register batches (Healthcare Product, Medications), etc

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All formulation services can be utilized independently or fully integrated within on-going services at Novick. It includes Process development and Optimization.

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GVK BIO offers an extensive Process R&D support, designed to address the issues involving both scientific and communication challenges. We are cognizant of the need for customisation as per client’s need.

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Olive healthcare is a fully integrated developer, manufacturer and marketer of broad range of soft gelatin formulations with a strong regulatory and infrastructure back end to support its r&d and growth strategy in global markets.

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Our expertise in scale up ensures that the final product will be suitable for large scale manufacturing & commercialization. We manufacture clinical trial materials, perform scale up batch manufacturing, with product transfer & validation services.

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Comprehensive evaluation of drug candidates during pre-formulation is critical to the formulation development process. Specific challenges include low bioavailability, poor solubility and/or permeability, and poor physical stability.

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Globela Pharma Pvt Ltd has uplifted our existing R & D facility, and installed fully functioning in house R & D center- with state of the art infrastructure, and experienced, skilled manpower.

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DPT provides comprehensive pharmaceutical research and development services focused on semi-solid and liquid dosage forms