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.

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