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Solubility Studies

Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
Polymorph Screening

Screen for unwanted API forms resulting from the drug formulation process.
Chemistry, Manufacturing and Controls (CMC)

Request Chemistry, Manufacturing and Controls services
LCMS Analysis

Physically separate substances using liquid chromatography and mass spectrometry.
Liquid Chromatography

Separate substances using a mobile and stationary phase.
Method Development and Validation

Develop and validate methods for synthesis and scale up of drug candidates.
Chemical Stability

Measure the stability of small molecules in solution.
NMR Structure

Determine molecular structure, identify chemical impurities and validate sample integrity.
Accelerated Stability

Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
Impurity Synthesis

Use high resolution MS or NMR to eliminate intermediates or organic byproducts and determine impurity content.
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