A comprehensive management of each project.
Rédaction médicale et évaluation clinique
Regular intervention of a clinical research associate on site throughout your study.
Effective management of your regulatory affairs.
Monitoring and coordination of the implementation of your clinical trials.
We handle the repayment of patients expenses.
Audits of good clinical practice in accordance with the law.
Qualified and experienced staff at your disposal.
We offer training for professionals or students.