Chemical and stability studies
Analytical studies to determinate active substances and impurities
- Analytical method set-up through the best approaches
- Set-up and validation of new analytical methods to identify and quantify active ingredients. or impurities (GC, GC-MS, HPLC-UV, HPLC-MS, ICP-OES, AAS, titration methods)
- Validation of methods provided by the customer
Stability studies
- CIPAC or ICH stability studies management (shelf life or accelerated)
- Storage and analysis of samples in climatic chambers for all required thermal-hygrometric conditions
For further information please contact us: pharma@eurofins.com