Clinical trial conduct
We deliver end-to-end clinical trial conduct services, supporting sponsors throughout the full clinical development lifecycle. Our integrated teams ensure efficient trial execution, regulatory compliance, and high-quality data generation across global and multicentre studies.
Our capabilities
Data management and statistics
IP and sample logistics
French Fast-Track for Phase I Clinical Trials
Our therapeutic areas
Over 1000 state-of-the-art trials
Over the past thirty years, we have gained extensive experience in Early Clinical Development across all therapeutic areas, from conventional FIH (First-into-Human) and phase I trials at our clinical trials unit, through to highly complex, specialised international multi-centre studies in the most challenging indications.
Types of trials
- Entry into man
- Entry into patients
- Proof of Concept (POC)
- PK/PD
- TQT (ICH E14)
- Absolute, Relative Bioavailability
- Bioequivalence
- Drug-Drug Interactions
- Proportionality
- Metabolism
- Food / Gender /Age effect
- Tobacco
- Vaccines
- Muscle Biopsy
- Micro-dosing
- Glucose Clamp
- Sleep Evaluation
- Biomarkers
Our laboratory
1, rue des Essarts, 38610 Gières, France
Supporting your clinical trials
Looking for a trusted partner to support your clinical trials? Let’s discuss how we can support your development programme.
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