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By using microfluidization technology process, Skyepharma provides preformulation / micronization solution to increase bioavailabity of poorly soluble APIs. It is also an interesting technology for micro and nano emulsion manufacturing.

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With expertise in characterizing and modifying a drug substances' physical, chemical and mechanical properties, our objective is to help you assess and choose the best solid form for progression into animal and human dosing trials.

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By rapidly screening excipients and selecting appropriate formulations, you can begin preclinical studies in a matter of weeks rather than months.

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To support API solid form R & D programs, we apply High-Throughput Screening Technology for discovery of new polymorphs, particle size engineering & development or automated crystallization scale-up development.

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Our Pre-clinical & Phases I & II services include pre-formulation, formulation development, analytical method development & evaluation, cleaning residue test, CTM lots testing, analytical method development & 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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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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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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Appco Pharma functions with a goal to deliver product development solutions to its clients that help them enhance the ROI of their drug development portfolio.

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AMRI's Process Analytical Technology (PAT) approach is consistent with the FDA perspective that quality cannot be tested into products, but should be built in.

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We have extensive experience in the testing of drug products from preclinical development to commercial drug products including preclinical prototype evaluation, Excipient compatibility, physical characterization, ICH stability testing of drug products.

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During the pre-formulation phase, Eurofins CDMO determines the physical & chemical properties of the API. Our team has experience with a wide range of different drug delivery routes, drug delivery systems and drug production technologies.

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Preformulation concept studies to accelerate your drug development and approval.

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Our dedicated team of scientists have their core training in the area of preformulation and have expertise in the complete pharmaceutical profiling of molecules.

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Early formulation development compliments Eurofins CDMO's IND enabling services through a targeted formulation design. Our scientists use strategies and technologies focused on bioavailability and steered by client's objective.

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Early phase formulation development to accelerate your drug development and approval.

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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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Formulation Development is the core activity at Zenvision Pharma and it includes Pre-formulation studies, formulation development, analytical method development & validation, stability studies, Dossier preparation & Technology Transfer.

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The R&D Department is staffed with fully trained and highly experienced scientists and has at its disposal state-of-the-art facilities striving to produce products according to GMP/GLP global standards.

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Innovative, non-toxic and fully biodegradable biopolymers, made of hydrophilic (PEG or modified PEG) and lipophilic (PLA, PLGA, CPL) blocks.

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Alternative to the use of inactivated viruses. Synthetic cationic polymers for nucleic acids (DNA or RNA) and hydrophobic APIs transfer.

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2D or 3D biopolymers that generate biodegradable dendrimers used in cosmetics and to vectorize an API or a fluorescent probe.