ISO 17025 Accredited Laboratory
Endotoxin (LAL) Testing
Essential safety testing for injectables and medical devices to ensure they are pyrogen-free.
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
Bacterial endotoxins can cause severe immune reactions. Our LAL (Limulus Amebocyte Lysate) testing services verify that your products are safe for in vivo use. We offer Gel Clot, kinetic chromogenic, and kinetic turbidimetric assays depending on sample sensitivity and interference profiles.
Technical Specifications
Kinetic Chromogenic LAL Assay
Gel Clot Method (Qualitative)
Inhibition/Enhancement Screening
FDA/USP Compliant Reports for IND submissions
Pyrogen-free water and reagent verification
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.