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Minakem provides fully integrated and technology-oriented contract manufacturing services ranging from process development, kilo lab & pilot scale-up through to full industrial scale manufacturing of complex molecules including HPAPIs.

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Our highly qualified professionals are working in product development, analytical development & IP rights. Our activities include Route Scouting, Process Development, Scale up, Technology Transfer, Synthesizing Impurities, Contract Research etc

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Our Pilot Plant is an independent building used for process validation, process scale-up and also for some small scale pilot production for lots of 15 to 50 kg.

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Bachem have the capacity to produce peptide APIs from gram scale up to annual quantities of hundreds of kilograms and small molecules APIs from gram scale up to annual quantities of tens of tons.

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Interquim S.A. has a pilot GMP plant, fully fitted with stainless steel, Hastelloy C and glass reactors with volumes ranging from 25 to 1,000 L and filtration, drying and final processing equipment suitable for all activities relating to scaling up.

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Pharmasynthese research and development laboratory offers a variety of services such as New molecule synthesis, Process development, Process industrialization and Scaling-up, Process Optimization and Troubleshooting and Custom manufacturing

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Pharmasynthese research and development laboratory offers a variety of services such as New molecule synthesis, Process development, Process industrialization and Scaling-up, Process Optimization and Troubleshooting and Custom manufacturing

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LEBSA has an active R&D department, a versatile GMP pilot plant, plus perpetually updated analysis and document services can be relied upon.

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MINAKEM's highly trained and professional research team develops new synthetic routes and supplies lab samples of new compounds or generic API's according to scalable and safe process. It also optimizes and scales up synthetic processes through lab work and pilot production.

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Wavelength delivers what you need when you need it. Our diverse multi-purpose production capabilities range from lab-scale (grams), through pilot scale (kilograms), to multi-ton commercial quantities offers cGMP scale up.

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Cayman's chemical synthesis capabilities includes total synthesis and scale-up of rare eicosanoids and their biologically active metabolites, specialized pro-resolving mediators and other complex fatty acids, sinefungin, emerging drugs of abuse, phytocannabinoids, and labeled versions thereof.

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ScinoPharm possesses a full range of chemistry capabilities & has extensive experience in synthesizing complex molecules. Depending on requirements, we develop new synthetic routes, or scale up & optimize processes based on the customer’s technology.

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Uquifa offers the opportunity to manage the development activities of any drug life cycle by offering services on DMF/CTD/COS application, stability studies, process validation and analytical method validation, working standard supply or impurity

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We have dedicated production area for manufacturing of general & bulk sterile substances with capabilities for Grams to Kilo scale & Pilot production. We have sophisticated QA, QC & PD lab supported with high-tech equipments.

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Dishman Custom Services, comprising both the CARBOGEN AMCIS and Dishman CRAMS businesses. We operate seamlessly across the entire lifecycle of a product, having an ability to manage projects from preclinical through to commercial scale manufacture.

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Flamma Honkai has R&D labs that allow us to do early stage, non-cGMP work for our customers. This approach allows fast service for small amounts of materials and eventual transfer to either our production plant in Dalian, China or our cGMP production facility in Italy.

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We optimize your lab protocol and develop the economically most reasonable synthetic route. Thereafter we scale up the method to a technical process and produce first quantities of up to several hundert kilograms in our piloting plant.

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Servier CDMO offers a full range of contract development and manufacturing services, from concept and product development to analytical testing, commercial scale and regulatory approval.

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CLEARSYNTH efforts focus from the pre-clinical stage through to phase III and to the successful technology transfer to manufacturing locations throughout the world.

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Scale-up facilities may be arranged either in Topchem Pharmaceuticals' own FDA inspected GMP facility or in collaboration with a leading Irish GMP manufacturer from kilos right up to multi-tonne scale.

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CTX Life Sciences has 83 reactors ranging from 0.1 m³ to 8.0 m³, with total reactor volume of 220 m³ and eight independent clean room areas. The supply of utilities and utility headers are isolated from manufacturing area to avoid congestion and cross contamination inside the plant.