Automate the manual, cumbersome and error prone processes and tools, not specifically built for study startup, for site selection, feasbility and activation in clinical trials.
goBalto Activate offers enhanced visibility into the traditionally cumbersome process of activating sites for clinical trials. The system creates efficiencies through streamlined communication among sites, sponsors and CROs. This ultimately drives shorter timelines and cost savings for our customers.
Alistair MacDonald, Chief Operating Officer,
Simplified with a single on-demand view, delivering instant status updates on study progress, irrespective of how many concurrent studies or vendors you work with.
Without oversight, a complicated protocol may not be interpreted correctly by the CROs, ineligible subjects may be recruited, and/or unqualified investigators may be employed.
Risk Identification & Mitigation
Reduce your clinical trial risk by deploying purpose-built study startup technologies that aid in risk management.
72% of studies run more than one month behind schedule, with sponsors standing to lose between $600,000 - $8 million for each day that the trial delays a product’s development and launch.
Discover bottlenecks and areas for process improvements with custom analytics and real-time metrics into on-going operations. Find out where to focus your efforts.
With our process improvement initiatives supported by goBalto’s Activate and Analyze solutions, we are able to deliver enhanced study start-up results, with median cycle time reduced by up to 25%.
Marie Keegan, VP and Global Functional Head, Study Start-Up,
Automate activities & document workflows with country-specific "smart" workflows that deliver global regulatory and SOP compliance.
The benefits of SOPs are clear, they provide a level of formal accountability for team members and they prevent noncompliance on a systemic level. But … they can’t help you if you don't use them.