Conquering the Complexity, Volume and Timelines
of Clinical Data Disclosure
Veritas Medicine created and launched the only scalable, fully integrated online compliance system available for your enterprise-wide use. The Veritas Clinical Trial Register (VCTR) can provide you with vastly improved efficiency and speed in the data posting process and full transparency into data posting status.
Basically, with VCTR you and Veritas Medicine create an ever-vigilant team keeping your clinical trials on schedule and in compliance every step of the way.
The major features of VCTR include:
- Role-based data entry limited by rigid data constraints to enforce compliance with ClinicalTrials.gov (CT.gov) and ClinicalStudyResults.org (CSR.org) requirements
- Workflow management that guides users through the data entry, review, and approval process
- Mitigates human error; maximizes “clean” data for submission
- Mitigates corporate compliance risk via full transparency
- Verifiable audit trail
- Ensures that all clinical trial data in the public domain is accurate and current at the same time
- Seamlessly integrates new compliance requirements based on current legislation
- Email notifications are also sent as Study Milestone dates approach, as protocols are updated, and as protocols move through the approval chain
- E-mail alerts are generated to notify relevant personnel of protocol data requiring internal review and approval
- All protocol summaries and study result reports (draft and final) are “tagged” to a Protocol ID number (associated with an NCT number assigned by CT.gov), for capture and tracking
- Veritas Medicine manages the posting of all approved data within the Clinical Data Posting Portal to the relevant external databases (via XML feed) on a weekly schedule
- Web Conference VCTR training for all relevant personnel
CONTACT US
Email: VCTR Sales