CanSaRCC's vision is to improve the outcome of patients with sarcoma. Our mission is to develop a comprehensive bioinformatics database and national network to capture high quality data. Our team works to accomplish this goal through a variety of clinical and scientific collaborations such as virtual biobanking, exploring patterns of disease, and collecting precise patient data.
We are proud to be the first registry in Canada to collect and aggregate both pediatric and adult sarcoma patient data