A leading player in Life Sciences
- Interventional studies: phases I to IV (medicines and medical devices);
- Non-interventional studies: observatories, epidemiological studies, PMCF, etc.
- Registries, data warehouses, etc.
Expertise that can be tailored to your needs
- Project leadership : Rigorous management, both strategic and operational.
- Monitoring 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.
- Support for AAP/AAC : Personalized support for your authorizations.
- Vigilance : Proactive management of adverse events.
- Digital solutions : Un développement sur-mesure pour chaque projet.
A daily commitment to innovation

- Good Clinical Practice (GCP),
- ISO 14155 standard for medical devices,
- GDPR for personal data protection,
- All applicable legislation.

