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Solubility Studies
Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
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Polymorph Screening
Screen for unwanted API forms resulting from the drug formulation process.
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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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Particle Size Analysis
Measure particle size distribution and characterize particle size, porosity and composition.
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Drug Product Stability
Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
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Analytical Development and Validation
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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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Dissolution Profiling
Measure release of API from formulation (tablet or capsules) under GMP guidelines.
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