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.