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By using microfluidization technology process, Skyepharma provides 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 substance’s 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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Development Process: Formulation of simple or highly complex products, Encapsulated in softgel dosage forms or other delivery systems, High or low potent APIs, Differentiated OTC products and nutritional supplements, Traditional and unique delivery systems

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

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At Quotient Sciences, we pride ourselves on providing the best analytical support, delivering candidate screening, drug product analysis and phase-appropriate method development and validation.

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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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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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Preformulation concept studies to accelerate your drug development and approval.

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During the pre-formulation phase, Eurofins CDMO determines the physical & chemical properties of the drug substance. In the formulation development phase, We assess different drug product concepts in terms of stability, efficacy & processability.

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

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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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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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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.

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Pre-formulation activities are one of the most crucial areas of the product development process. These activities determine which process and delivery methods will provide the most stable form of the drug.

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We provide full range of analytical services, State-of-the-art instruments, cutting-edge technologies, and experienced scientific staff ensure efficient, high-quality and cost-effective services.

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Crystallics has capabilities to determine powder properties like bulk and tap density, flow properties, odor & color, electrostatics, compression properties, compaction properties, milling, grinding & granulation (chemical physical stability).

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Based on more than 30 years of experience and application with an extensive range and type of products, our customers gain more knowledge, Innovation and technological expertise through the following services: pre-formulation for early safety studies.

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Bluepharma currently has the capability for the development of potent drugs, from the initial steps of the development until the manufacturing of submission batches.

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Whether it is a New Chemical Entity or a mature API, Galenix can help with the characterization and the building up of the Drug Master File (DMF) which is deemed necessary for the final registration process.

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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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All formulation services can be utilized independently or fully integrated within on-going services at Novick. These services include Pre-formulation Development.

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Starting with DOSE™, our own preformulation system and proceeding through formulation, production for pre-clinical toxicology, scale up and clinical trial material production, Particle Sciences is expert at efficiently getting our clients to commercializable products