In order to obtain the highest quality for your clinical studies and optimize the timeline, we have entered into partnership with two clinical centers.Clinical trials are performed in close collaboration with these trustworthy clinical units, all of which are recognized by International or European Authorities (FDA, ANSM, WHO, MHRA …). All trials are conducted in compliance with applicable Good Clinical Practices (GCP) and safety measures.

Benefits of full clinical services:

Benefits of ADME clinical services

Human pharmacokinetics: phase I

Design the optimal study for your project from preclinical data

Human Pharmacokinetics including clinical and bioanalytical services:
Development and validation of bioanalytical methods (according to FDA and EMA Guidelines)
  • Sample bioanalysis
  • Pharmacokinetics – Kinetica® 5.1 version and WinNonlin® 6.4 version
    • Calculation and interpretation of pharmacokinetic parameters
    • Statistical analysis
  • Complete study report

For further information please visit Bioanalytical support

Human pharmacokinetics: phases II/III
  • Comprehensive central lab facilities and capabilities
  • Therapeutic drug monitoring
  • Pharmacokinetic modeling, including population PK and PK/PD

For further information please contact us.


We offer attractive packages to help you complete your bioequivalence studies rapidly and successfully.
Eurofins Leader group in analysis, associated with competitive CRO to provide you with BE solutions

For more details about clinical centers, please contact us.

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