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We also provide solubility-enhanced dosage forms including amorphous (spray-dried, HME) dispersion in a bottle, Lipidic vehicles such as Self-emulsifying & microemulsifying drug delivery systems, micronized API in a bottle, capsule or tablet format.

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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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We also provide solubility-enhanced dosage forms including amorphous (spray-dried, HME) dispersion in a bottle, Lipidic vehicles such as Self-emulsifying & microemulsifying drug delivery systems, micronized API in a bottle, capsule or tablet format.

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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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We also provide solubility-enhanced dosage forms including amorphous (spray-dried, HME) dispersion in a bottle, Lipidic vehicles such as Self-emulsifying & microemulsifying drug delivery systems, micronized API in a bottle, capsule or tablet format.

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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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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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We also provide solubility-enhanced dosage forms including amorphous (spray-dried, HME) dispersion in a bottle, Lipidic vehicles such as Self-emulsifying & microemulsifying drug delivery systems, micronized API in a bottle, capsule or tablet format.

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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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We also provide solubility-enhanced dosage forms including amorphous (spray-dried, HME) dispersion in a bottle, Lipidic vehicles such as Self-emulsifying & microemulsifying drug delivery systems, micronized API in a bottle, capsule or tablet format.

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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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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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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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We have 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