The BIOMIC_AUTh group can provide expert GLP & Non-GLP analytical services using LC-MS/MS and GC-MS/MS technology.
- Experience in development, validation and application of quantitative analysis of drugs, drug metabolites and endogenous metabolites in virtually any biological specimen.
- Quantitative bioanalytical method development
- Bionalytical method transfer
- Full method validation according to guidelines (FDA recommendation to industry)
- Clinical/biological sample analysis
- Data treatment and integration
- Clinical research support
- Support from drug discovery to drug development and clinical trials.