Our Services

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Comprehensive support of preclinical and clinical studies in full compliance with regulatory guidelines using LC-MS/MS, including:

• Method development or method transfer
• Method validation
• Sample analysis

Rapid method development and sample analysis to support discovery in all types of biological matrices, including:

• Method development or method transfer
• Method qualification
• Sample analysis

Full execution of plasma protein binding studies in humans during drug development process, including:

• Ultrafiltration and equilibrium dialysis
• Evaluation of extent of binding to plasma proteins

Range of consulting services offered to large, mid-size, and small pharmaceutical companies, including:

• Management and oversight of CRO bioanalytical studies
• Mock regulatory inspections and training
• IND application review