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Drug Formulation

Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
Polymorph Screening

Screen for unwanted API forms resulting from the drug formulation process.
API Physical Characteristics

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

Store and track biological samples.
Excipient Compatibility

Test excipients for drug formulation, effects of temperature, time, humidity, pH and light exposure as well as excipient release.
Salt Form Selection

Use high-throughput automated arrays to combine APIs with multiple salts and ions to optimize formulation.
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.
API Stress Testing Studies

Develop analytical methods to predict stability problems and identify degradation products/pathways under forced degradation conditions.
Excipients

Acquire synthetic or natural inert components to formulate therapeutic agents.
Tablet Manufacturing

Use automatic or semi-automatic machinery to create various standard and non-standard tablets.