Products
Trialpoint™CTMS
Clinical Trial Management System
Take control of your clinical trials
A well designed clinical trial managment system allows you to accelerate your study start-up, effectively communicate with your clinical sites and research team, and track all trial milestones any time any place.
Basic features
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Complete study budgeting and financial management tools with automatic revenue accrual
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Real-time tracking of study milestones and regulatory documents
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Graphical scheduling for staff and patient appointments
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21CFR Part 11 and HIPAA compliant
Reporting
A wide selection of standard reporting tools and custom templates lets members of the research team find the information they need quickly.
TrialPoint™CTMS standard reporting templates include:
- Site enrollment rates
- Subject screening/enrollment rates
- Follow-up visit rates
- Study schedules
- Safety reports
- Monitoring
- Investigator grant payments
IRB module
The IRB module allows the sponsor and site personnel to:
- Submit and track all protocol submissions, IRB approvals, correspondence and regulatory documents electronically
- Set automated reminders
- Improve compliance with adverse event reporting