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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
Liquid Chromatography

Separate substances using a mobile and stationary phase.
Non GLP Small Molecule Bioanalysis

Detect and analyze the pharmacokinetic profile of small molecules.
Accelerated Stability

Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
Drug Product Stability

Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
Bioequivalence Studies

Assess the expected biological equivalence of two proprietary preparations of a drug.
API Physical Characteristics

Characterize physical and chemical properties of new drug molecules to develop safe, effective, and stable dosage forms.
Product Testing

Ensure product quality standards are met.
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