At CVTA we perform: optimization and development of analytical methods, studies of accelerated stability, validation and transfer of analytical methods and GMP analytics. We also perform qualitative and quantitative analyses of various (mostly pharmaceutical) products with validated analytical procedures in the GMP environment. We also issue certificates of conformity. Analytical techniques available at CVTA: UV-VIS, HPLC, UPLC, GC, dissolution tests, ICP-MS, ICP-OES, IC, He-Pycnometry.
CVTA maintenans, develops and educates for work within the GMP system for all departments and laboratories of KI.
- GRIČAR, Maja, ANDRENŠEK, Samo. Determination of azide impurity in sartans using reversed-phase HPLC with UV detection. Journal of Pharmaceutical and Biomedical Analysis, 2016, 125, 27-32.