CRS Service

Analytical Development & Validation

Accurate, reliable, and reproducible analytical testing across the drug development lifecycle.

Physical & Chemical Testing

Robust analytical methodologies using HPLC, GC, and LC-MS for precise characterization and quality assurance.

Stability Studies

Evaluation of shelf life and integrity under diverse environmental conditions.

Dissolution

Dissolution testing to evaluate release profiles, support optimization, and meet regulatory requirements.

Method Development

Discriminating dissolution, particle size analysis, residual solvent testing, and other advanced analytical techniques.

Method Validation

Validated methods that support consistent product quality, safety, and regulatory expectations.

Impurity Profiling

HPLC, LC-MS, and GC-MS techniques identify and quantify impurities against stringent standards.