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Solubility Studies

Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
Drug Formulation

Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
Chemistry, Manufacturing and Controls (CMC)

Request Chemistry, Manufacturing and Controls services
Drug Product Stability

Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
Forced Degradation

Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
Dissolution Profiling

Measure release of API from formulation (tablet or capsules) under GMP guidelines.
API/ Excipients Compatibility Studies

Delineate real and possible interactions between potential formulation excipients and the API as an important risk reduction exercise early in formulation development.
Excipients

Acquire synthetic or natural inert components to formulate therapeutic agents.
Drug Substance and Drug Product Characterization and Manufacturing

Drug Substance and Drug Product Characterization and Manufacturing.
Spray Drying

Convert a liquid into a powder by rapidly drying the mixture and removing the moisture component.