The Trialogics team understands the different different needs for site, sponsor, and patient workflows as they relate to different study areas. We configure your system so it helps you meet your goals faster.
We link IRT with ePRO and wearables, or other key technology. Integration helps you accelerate FDA submissions and to improve the accuracy of data and produce reliable patient safety information.
Visualize data with bar charts and pie charts, not just complicated spreadsheets. Real-time
advanced reporting helps you turn insights into decisions.
Call a local support representative
at any time to help resolve technical issues and speed up your clinical trial.
The Trialogics team trains clinical trial staff on the software at your trial site. When clinical teams that are more comfortable with the software, they can extract better insights from the system.
Development, testing, validation, implementation, and support adheres to the FDA’s strict software regulation guidelines. Trialogics utilizes Microsoft’s Worldwide Azure data centers for backup and
Our team has experience successfully launching clinical trial software in a number of therapeutic areas. We optimize your system to meet your study requirements.