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
- Complete study budgeting and financial management tools with automatic revenue accrual
- Real-time tracking of study milestones and regulatory documents
- Graphical scheduling for staff and patient appointments
- 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 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
If you would like to know more about TrialPoint™CTMS or have a project you would like to discuss please call 845 278 0576 or email us.