Study management and reporting

Our operational team is the first point of contact between the sponsor and the investigation site. Our clinical project managers are experienced in phase I/II trial execution and implementation. They have a deep understanding of the specific project dynamics and study objectives, and supervise:

  • SAE monitoring and follow-up;
  • coordination of data management teams, bioanalytical laboratories and other partner’s activities;
  • writing, coordination and review of clinical study reports;
  • respect for study timelines and budget; and
  • essential study document track records.