Where a successful trial launch begins its ascent
Optimize and automate data collection. Fast, efficient, and accurate trial management. Ensures quality from project start-up to study closure.
- Automates the study start-up process
- Templates provide critical regulatory knowledge
- Project management approach to document collection
- Meets timelines by focusing on critical path items
- Easy configuration with no costly customizations
- Increases end-to-end visibility of study lifecycle
- Enhanced communication between CROs and sponsors
- Process optimization eliminates bottlenecks and creates accountability
- Easier compliance through eTMF integration
- Activity and document tracking
- Site identification
- Site selection
- Country-level approval tracking
- Site initiation and IP
- Predefined country docs and regulations
- Pre-loaded experience tables and metrics
- Feasibility, contracts, and submissions
- Pre-populated country requirement templates
- Fully configurable
Study Start-Up + CTMS
Eliminate communication gaps and missed triggers between startup and clinical groups. No more relying on email and spreadsheets for crucial site qualification visits and site initiation visits.
Study Start-Up + RBQM
Launch your study with data quality and risk mitigation in mind. Quickly collaborate with your team and gain the visibility you need for effective startup and quality control.
Study Start-Up + RBQM + CTMS
Take your clinical trial to the next level by adding RBQM. Now you can effectively manage your study data from the first site identification to the last patient visit.