ECH Santé supports medical institutions with all the tasks related to clinical trials. Our motto: LET THE HEALTHCARE PROVIDERS FOCUS ON THEIR PATIENTS

Clinical trials represent an opportunity for patients care, but the administrative complexity can be a burden for the medical staff. ECH Santé supports your trials so that clinical research remains an asset for the patients and their healthcare providers:

  • Data entry into the study CRF.
  • Coordination with the sponsors / administrative paperwork
  • Rationalisation des tâches liées à la recherche clinique à l’échelle de l’établissement
    • team coordination
    • préparation des documents d’aide au recueil de données
    • worksheets
    • staff training and protocole follow-up



Extensive experience in the different areas of medical research (regulation, monitoring, coordination)


Guy Teissier, managing director

  • 6+ years clinical research experience within international Clinical Research Organizations
  • Monitoring/coordination of Phase I to III trials within numerous therapeutic areas (Oncology, Cardiology, Endocrinology, Neurology, Hematology...)
  • Expérience sur des études complexes (pédiatriques, génétiques)
  • International standard expertise in ICH-GCP and local regulations IT proficiency and workflow optimization
  • IT Proficiency and workflow optimization skills
  • Relationship skills with investigators and medical staff