Precision.
The difference between a failed batch and a blockbuster drug. We are the partner pharmaceutical innovators trust for definitive analytical proof.
Analytical Excellence
Specialized testing services for the biopharmaceutical lifecycle. From R&D to lot release.
Peptide Purity Analysis
High-resolution analysis of peptide synthesis products. We detect impurities down to 0.01% using UPLC-MS.
- Molecular Weight Confirmation via MS
- Purity % Calculation (Area Under Curve)
- Impurity Identification & Characterization
Small Molecule / Drug Analysis
Rigorous testing for APIs (Active Pharmaceutical Ingredients) and drug formulations.
- Potency Verification against Reference Standards
- Degradation Product Analysis
- Solubility & Stability Testing (pH, Temp, Light)
Endotoxin (LAL) Testing
Essential safety testing for injectables and medical devices to ensure they are pyrogen-free.
- Kinetic Chromogenic LAL Assay
- Gel Clot Method (Qualitative)
- Inhibition/Enhancement Screening
Why Top CDMOs Choose Genvlab
Data You Can Defend
We don't just run samples; we validate results. Our Certificate of Analysis (CoA) stands up to the most rigorous FDA and EMA scrutiny.
Ph.D. Level Support
Direct access to analytical scientists who understand your molecule's unique chemistry, not just account managers.
Method Lifecycle Management
From early-stage feasibility to late-stage validation (USP <1225>), we support your method's entire journey.
24h Turnaround Available
For critical lot release testing, we offer expedited workflows without compromising data integrity.
Ready to Validate Your Science?
Start your sample submission online. Our secure portal ensures data confidentiality from submission to result.
Genvlab's structural elucidation of our impurity profile was the turning point for our IND submission. They identified a degradation product that three other labs missed.