A benchmark player in life sciences
- Interventional studies: phases I to IV (drugs and medical devices) ;
- Non-interventional studies: observatories, epidemiological studies, PMCF, etc.
- Registers, data warehouses, etc.
Expertise tailored to your needs
- Project management : Rigorous management, both strategic and operational.
- Follow-up and investigation : A team of experienced and committed ARC professionals.
- Biometrics and data management: Reliable management and analysis of all your data.
- Regulatory affairs : drafting documents and submitting them to the authorities.
- AAP/AAC support: Customized support for your authorizations.
- Vigilance : proactive management of undesirable events.
- Digital solutions: Tailor-made development for every project.
A daily commitment to innovation

- Good clinical practice (GCP),
- ISO 14155 standard for medical devices,
- GDPR for the protection of personal data,
- All applicable legislation.



