How do we help?
- Improve speed and accuracy – automate submissions to ClinicalTrials.gov using validated fields.
- Work more efficiently – slash data entry, review, and approval times by up to 85%.
- Collaborate with confidence – work whenever, wherever with field-level commenting and verified e-signatures.
- Report your way – choose from predefined templates or ad-hoc creation.
- Meet deadlines with ease – keep track of due dates with our proprietary disclosure rules library.
- Tighten up your team – clarify tasks and timelines with role assignments and configurable workflows.
- Always be audit ready – you’re well prepared with our full log conforming to 21 CFR Part II/Annex 11.
- Repurpose trial data – sync your data across forms and registries.
It can help you to:
- validate your data against field-level registry requirements.
- evaluate your trials to determine what must be disclosed, on which registry, and by what date.
- alert you of impending deadlines and can be modified to match internal policies/business rules.
- Prepare, Edit, Review, Approve and Submit data for multiple registries in one central form
