We consider our Regulatory Document Coordinators (RDCs) to be among the best in the industry. Rarely do we get a query from Monitors in this department. The RDCs maintain all regulatory documents in compliance with IRB and FDA requirements. From the initial submission to the very last correspondence, we have strict SOPs that require immediate turn-around and accuracy. Part of our regulatory process requires the clinic team to follow the same system of accountability to ensure that current consent forms are administered and new amendments are implemented the same day/time posted. RDCs also process and track the Confidential Disclosure Agreement and Clinical Trial Agreement. Our average turn-around time in this department is 1.5 days.