The Casey Reading Center has gained significant regulatory and organizational experience by being the primary reading center in dozens of ongoing clinical trials. We understand there is a strong need for a reading center that can work directly with commercial and academic organizations to design clinical trials, particularly as the options for primary and exploratory endpoints becomes more extensive and nuanced.  

We believe that designing an efficient trial from "end to end" will allow time and cost savings later.

CRC provides an efficient certification, data transfer and feedback.  

Thus, we work with sponsors, contract research organizations, academic institutions and instrument manufacturers to develop standard data analysis requirements to use images and functional testing for study eligibility, treatment criteria and end point analysis.