How It Started
As clinical research has grown as an industry, so has it grown in oversight, regulations, and sponsor/CRO expectations for research sites. As a result, study-to-study and site-to-site, we noticed a separation between what sites were able to accomplish and what monitors expect from their sites.
On the site-side, this has led to research sites underperforming, creating headaches for their overburdened monitors, or worst of all, cutting important ethical/regulatory corners to deliver questionable data to sponsors/CROs. On the sponsor side, this has led to delays in trial timelines, a shrinking pool of clinics able to meet their needs and loads of data to investigate and clean up throughout the process.
After years of experiencing this at the clinic, sponsor, and CRO levels, a group of like-minded colleagues connected to form the base of what would be CNB Clinical Research under one goal: addressing this growing disconnect between sponsor/CRO requirements and the everyday demands of principal investigators and their clinics and streamlining the process as a whole.
