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Quotient Sciences has almost 30 years of experience developing a breadth of formulations across a range of indications.

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It is a complexation process to improve the solubility and bioavailability of a poorly soluble active ingredient, This complexation process by cyclodextrins differs from other complexation processes. It is performed in supercritical CO2 medium.

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Glatt can optimize the active substance release and bioavailability by specific optimized formulation and process methods depending on the physico-chemical property of the active substance.

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Solubility screening, bio-availability enhancement to accelerate your drug development and approval.

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Quotient Sciences has almost 30 years of experience developing a breadth of formulations across a range of indications.

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The Glatt MicroPX™ technology (micro pelletizing technology) is a continuous fluidized bed agglomeration procedure for the manufacture of pellets and micropellets with a very high active ingredient content.

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Quotient Sciences has almost 30 years of experience developing a breadth of formulations across a range of indications.

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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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With over 40% of new drug substances exhibiting poor aqueous solubility, a major task for industrial pharmaceutical scientists has been to explore alternative procedures for overcoming this characteristic which can compromise the bioavailability, and thereby detract from optimising the clinical

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Quotient Sciences has a proven track record of developing and manufacturing SDDs to overcome your poor drug solubility and delivery challenges. We tailor the development of your SDD toward the specific physical and biopharmaceutics properties.

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Capsugel is a leader in drug solubility and enhancement of solubility or dissolution rate. The depth of our bioavailability enhancement technologies makes Capsugel a leader in enhancing drug solubility and drug dissolution rate.

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With nearly 30 years of experience, Quotient has established a broad suite of technologies and formulation approaches including amorphous dispersions and lipidic formulation development.

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Custom’s expert chemists, scientists and process engineers — many with 35 years of experience in the pharmaceutical industry — offer an extensive range of clinical and product development expertise, including significant preformulation and formulation exp

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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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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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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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GRAM Laboratories offers services for conduct of preformulation studies. These studies are physical and chemical characteristics of the active ingredient of pH-solubility-stability profile, evaluation of solubility in various matrices and moisture uptake studies-hygroscopicity.

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AbbVie advances your science like we would our own, with customized pharmaceutical hot melt extrusion services that include solubility/bioavailability enhancement.

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In the analytical development area, LABIANA GROUP offers a wide range of services for pharmaceutical and veterinary industries and provides study of solubility in different media.

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Characterization studies for your product can be conducted prior to formulation. We specialize in the design and execution of pertinent pre-formulation activities required for successful pharmaceutical product development.

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Particle Sciences has developed a proprietary approach to solubilization using a combination of computational tools and empirical data. DOSE has resulted in several clinical products already and is the basis for much of our work.

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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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GVK BIO offers preformulation services such as Intrinsic Dissolution

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GVK BIO offers preformulation services such as solubility (aqueous, non-aqueous, FaSSIF, FeSSIF and SGF mediums)

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GVK BIO offers preformulation services such as pH-Solubility profile

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GVK BIO offers preformulation services such as Impact of Particle Size on Dissolution

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AvacaPharma's scientific team has an up to date understanding of product development aspects. Analytical scientists focuses on method development, validation, instrumentation, technology transfer and stability studies.

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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.