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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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Method Development and Validation
Develop and validate methods for synthesis and scale up of drug candidates.
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Chemical Stability
Measure the stability of small molecules in solution.
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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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Photostability
Measure drug degradation rates after exposure to various light sources.
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Forced Degradation
Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
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Dissolution Profiling
Measure release of API from formulation (tablet or capsules) under GMP guidelines.
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Excipient Compatibility
Test excipients for drug formulation, effects of temperature, time, humidity, pH and light exposure as well as excipient release.
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