R&D Services
Preclinical & Non-Clinical Studies
Preclinical done right — in our own GLP facility.
A state-of-the-art GLP research facility built for regulatory-grade non-clinical work.
What’s included
- General toxicology, pathology, developmental & reproductive toxicology
- Geno-toxicology (in-vitro & in-vivo); environmental & aquatic toxicology
- ICCVAM/ECVAM/OECD-approved alternative methods; validated efficacy (PoC) models
- Biocompatibility for devices (ISO 10993, OECD GLP); stability, method development, impurity profiling, 5-batch testing
Why CEBIS
We own the facility — a Class 100,000, 24/7-monitored GLP environment with individual AHUs, pressure-gradient design and isolated procedure rooms. Preclinical is designed backwards from your regulatory goal, and the same organization carries your molecule into first-in-human without a hand-off.