ISO 17025 Accredited Laboratory
Method Development
Custom analytical method development and validation for novel compounds.
24h Turnaround
FDA Compliant
99.9% Accuracy
Retention Time 12.45 min
Area % 99.98%
Mass Error 0.2 ppm
✓
Batch Released Authorized by QA
Overview
When standard methods aren't enough, our PhD-level scientists develop robust analytical methods tailored to your specific molecule. We validate methods per ICH Q2(R1) guidelines, covering specificity, linearity, accuracy, precision, range, and robustness.
Technical Specifications
Custom Method Optimization for tough separations
Validation Protocol Design
Linearity, Accuracy & Precision Studies
Limit of Detection (LOD) / Limit of Quantitation (LOQ)
Full Technology Transfer Packages
Methodology & Compliance
All analysis is performed under strict ISO 17025 accredited SOPs. Our instruments are calibrated daily, and system suitability is verified before every run. Final reports include full chromatograms, spectral data, and raw data files upon request.