Core Functions

Clinical Data Capture

With TEMPO's Clinical Data Capture features, conducting post-approval research and drug, patient or disease registries has never been easier. Flexible in design and capable of supporting thousands of investigator sites, TEMPO can scale to meet the demands of the largest studies. Additionally, data verification and cleaning functions are streamlined at the point-of-entry through a web-based interface, and TEMPO's patented and fully integrated randomization function removes the headache of dialing into an IVR system.

With TEMPO, site investigators can capture data faster and with greater accuracy and quality than ever before.

Study Management

With TEMPO's Study Management features, implementing and monitoring post-approval research and drug, patient and disease registries has never been more efficient and effective. TEMPO's online protocol and system training functions get investigators and their staff up-and-running quickly. This not only saves money, but ensures study conduct occurs according to protocol while following GCP guidelines. Study monitors also have immediate access to data as it's entered, plus the ability to identify and resolve data discrepancies remotely. These functions enable critical decision-making for all stakeholders by creating transparency into enrollment, site management, investigator payments, milestone tracking and more.

With TEMPO, trial monitors and project managers activate sites quickly and keep projects on pace, while maintaining constant vigilance over study conduct.