The quality of the products we deliver is fundamental. Accordingly, Eurogentec has maintained a Quality Management System that ensures each employee always operates in respect to standard procedures and fulfills our global quality policy.
QC for biopharmaceuticals
Our large QC department is responsible for testing and monitoring of the environment, the incoming raw materials, the production suites, and performing ICH based stability studies.
QC for chemicals
QC analytical methods are qualified for raw material and final product release to meet your specifications.
- Appearance, pH, Osmolality
- Purity by UPLC / HPLC, Bioburden, Endotoxin level
- Identity by Mass Spectrometry (ESI), Sequencing
- Stability studies
- Residual solvents, Residual heavy metals, Water content, Sodium content
- Phosphorothioate - Phosphate content
Discover our Therapeutic Oligos service
QC for enzymatically synthesized molecules
QC methods for Transfer, Development and Optimization including
- RT-PCR and qPCR
- ELISA and Dot Blot
- Endotoxin and residuals measurements
Discover our IVT-RNA service