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Polymorph Screening

Screen for unwanted API forms resulting from the drug formulation process.
Solubility Studies

Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
API Physical Characteristics

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

Crystallization studies
Excipient Compatibility

Test excipients for drug formulation, effects of temperature, time, humidity, pH and light exposure as well as excipient release.
Differential Scanning Calorimetry

Elucidate the thermodynamics associated with conformational transitions.
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.
NMR

Determine molecular and protein structure, and validate sample integrity.
Accelerated Stability

Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
Denaturing High Performance Liquid Chromatography

Separate mixtures of denatured and reannealed oligos to identify single nucleotide substitutions, deletions and insertions.
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