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Drug Formulation
Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
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Chemistry, Manufacturing and Controls (CMC)
Request Chemistry, Manufacturing and Controls services
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Accelerated Stability
Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
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Drug Product Stability
Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
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API Physical Characteristics
Characterize physical and chemical properties of new drug molecules to develop safe, effective, and stable dosage forms.
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Photostability
Measure drug degradation rates after exposure to various light sources.
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Bulk Manufacturing
Find facilities for large-scale mass production.
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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.
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API Stress Testing Studies
Develop analytical methods to predict stability problems and identify degradation products/pathways under forced degradation conditions.
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Tablet Manufacturing
Use automatic or semi-automatic machinery to create various standard and non-standard tablets.
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