Our proven comprehensive site support model involves placing a full-time, highly qualified clinical research coordinator at each study site to assist the investigators and site staff with all day-to-day study conduct activities. In addition, weekly teleconferences are scheduled with the site throughout the project that allows our staff to review study status, CRF and query completion and assist with protocol questions and any other study related activities to ensure the study proceeds in a timely manner. Croissance Clinical Research ensures all study information is current, prioritized, and available to Sponsors for effective site management.
Croissance Clinical Research is a Bio pharmaceutical Service provider and full service CRO, providing services to pharmaceutical, biotechnology and medical devices companies. We apply our innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R&D investments.