Starting with the end in mind, we work shoulder to shoulder with your team to define exactly what, where, when, and how your study data will be collected, cleaned, and made available for meaningful analysis. Within weeks, we turn your study specifications into a validated clinical data collection tool available around the clock, and around the world.
Our team of experienced eCRF/database designers will create templates that accurately capture the protocol-required data. The resulting input documents will be designed to look like traditional paper forms. This approach enhances the data entry experience for site personnel and assures a pleasant user experience with our intelligent eCRFs.
Our staff of experienced database and data management professionals work directly with your team to create the specifications needed to build your study database. This includes specifying the built-in logic checks to ensure the most robust data capture by providing real-time feedback as data is entered. The result will be a logical database schema designed to support your unique data collection and analysis requirements.
We pre-qualify potential investigational sites to assure their ability to successfully utilize our technologies. This process helps to establish regulatory compliance and promotes a positive end-user experience.