ISO 17025 Accredited Laboratory
Small Molecule / Drug Analysis
Rigorous testing for APIs (Active Pharmaceutical Ingredients) and drug formulations.
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
Ensure the identity, potency, and purity of your pharmaceutical compounds. Our Small Molecule Analysis service adheres to strict quality control protocols suitable for R&D and pre-clinical studies. We specialize in forced degradation studies and stability testing to predict shelf-life and identify potential degradation pathways.
Technical Specifications
Potency Verification against Reference Standards
Degradation Product Analysis
Solubility & Stability Testing (pH, Temp, Light)
Dissolution Profiling for solid dosage forms
Residual Solvent Analysis (USP <467>)
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.