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Drug Formulation

Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
Chemistry, Manufacturing and Controls (CMC)

Request Chemistry, Manufacturing and Controls services
Method Development and Validation

Develop and validate methods for synthesis and scale up of drug candidates.
Chemical Stability

Measure the stability of small molecules in solution.
Accelerated Stability

Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
Drug Product Stability

Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
Forced Degradation

Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
Photostability

Measure drug degradation rates after exposure to various light sources.
Dissolution Profiling

Measure release of API from formulation (tablet or capsules) under GMP guidelines.
Real-time Stability Test

Assure stability and physical integrity of consumer products in real-time conditions.
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