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Method Development and Validation

Develop and validate methods for synthesis and scale up of drug candidates.
Analytical Development and Validation

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Melting Point

Use melting point analysis to characterize compounds based on calorimetry and thermodynamic data.
Compound Integrity

Analyze the identity and purity of small molecule drug candidates.
API/DP specific test methods

API/DP specific test methods (e.g., stability indicating HPLC assay and purity)
UV and IR Profiling

Analyze the integrity of a compound or large biomolecule.
Excipients

Acquire synthetic or natural inert components to formulate therapeutic agents.
Compendial test methods

Run Compendial test methods (e.g., KF)
USP <62> Microbial Limits Test

Determine the presence or absence of specific microorganisms.
USP <61> Microbial Limits Test

Determine whether a substance or preparation complies with an established specification for microbiological quality.
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