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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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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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We provide a comprehensive range of development services from feasibility studies to full formulation development and scale-up of complex oral formulations, designed to meet a wide range of delivery profiles and using proven technologies.

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Drug’On serves as CMDO and Technology Transfer for API and API intermediates. In the last year Drug’On improved its activities relating to opioids, anesthetics and antidepressants.

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Dishman's provides efficient technology transfer either between the customer and Dishman or between the Dishman Group sites. For technology transfer, a specialist team follows an established three stage procedure.

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We have proven expertise in technology transfers, product launches, product development and manufacturing technologies. Our Phase-III services include Tech-transfer, scale up, process / cleaning validation, etc

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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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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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Our team of QPs from diverse backgrounds can assist in all aspects of technology transfer, helping you save time and costs.

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Alven's R&D team focuses on the process development and specializes in the transfer of technology from the laboratory scale to the pilot plant scale. This knowledge is used for the development of branded and generic API’s as well.

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Seamless technology transfer from lab to pilot-plant and to commercial plant for large-scale manufacturing

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Capua BioServices has extensive experience in working with customers on projects from all over the world. The main expertise of Capua BioServices in pharmaceutical services relates to technology transfer and the manufacture of small molecules, recombinant

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Our experienced team makes it easy to take the formulation from lab to the commercial scale during the technology transfer process.

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DELORBIS provides contract manufacturing for many customers. This includes the entire technology transfer of our customers’ products to our manufacturing facilities, in accordance to their dossier requirements.

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UPM’s analytical group has a diverse background in analytical method development and in-depth understanding of all facets of the drug development process.

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PSR has capabilities and experts to allow the performance of technology transfer tasks to various global manufacturing sites for the purposes of scale up and commercializing various products forms.

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Crenza is a full scale R&D centre for development of Parenteral and Ophthalmic drug products. Crenza is founded by Industry professionals with invaluable experience and proven track record of development and commercialization of Parenteral and Ophthalmic drug products for regulated markets.

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Product life cycle scalability of formulations (early pilot studies, clinical trial materials, commercial batches), technical transferability are assured at all times thanks to a seamless collaboration between our development and manufacturing teams all on one site.

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Process scale up and technology transfer-We are one of the few companies in fluorination chemistry with the experience, capability and expertise in scale up from researchnto pilot and manufacturing.

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We offer full service solutions and project management for cost effective product development in pharmaceutical as well as food /nutraceutical areas.

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Curida AS is involved in manufacturing of bottles since 1974 with scalable production capacity to 12 milllions units dealing in Solutions, emulsions and suspensions. We also have experience with products containing ethanol, up to 32 %; Pilot equipment for tech transfer and clinical batches.

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