Each study is set up in our Global Results Database which is accessible through our Data Portal to enable data consistency and standardized reporting (upon Sponsor’s request). The real-time system allows standardized global reporting of laboratory data to Sponsors and CROs, as well as the production and organization of management reports. The main purpose of our Data Portal is to provide 24-hour, secure access to authorized data reports and clinical trial information. Different access levels are deployed to accommodate Sponsors, Monitors and Investigators. In addition to the Standardized Reporting Tool, several Management Reports and Query Tool Reports are also available.