Start-up is a crucial time in any clinical study. It can also be chaotic. Developing protocols, choosing sites, onboarding patients—every step can have a profound impact that ripples through the length of the trial. Mistakes can take months to uncover—and then totally derail or significantly delay a trial.
Although increasingly complex trial designs have led to increasingly complex start-up activities, more than 81% of operations teams still use spreadsheets to organize their study start-up. That’s time-consuming, susceptible to human error, difficult to troubleshoot, obstructive to regulatory compliance—and the need for multiple hand-offs creates a lack of immediacy that slows decision making.
Remarque saw an opportunity to streamline the process. Its Study Startup (SSU) application automates collection of all trial data, then optimizes that data to decrease cycle times and intervals between steps. That minimizes errors and compresses timelines. Step-by-step, this webinar will explore how Remarque’s approach to SSU eliminates bottlenecks, improves quality and increases visibility.
• Centralized document tracking supports collaboration
• Workflow management highlights critical path items, helping prioritize tasks, meet timelines, and ensure consistency.
• Built-in templates simplify country-specific regulatory compliance
Finally, with a real world example, learn how SSU helped a large CRO move a crucial phase three trial to launch in less than a month.