Trialpoint™EDC
What is TrialPoint™EDC
TrialPoint™ EDC is
a 21 CFR Part 11 and HIPAA compliant electronic data capture system that provides real-time
data collection functionality and reporting tools critical to today's demanding clinical trial industry.
Ultra-Fast Solution
TrialPoint™ EDC allows you the flexibility to quickly set-up and deploy investigational protocols, add or make changes to case report forms mid-trial, issue and manage data corrections, view real-time safety reports, and to close the database minutes after the last patient has completed the study. If you don't have the time, experience or resources to dedicate to electronic data management let our team be your guide for a full service EDC experience.
Cleaner Data
To keep your data clean and accurate, TrialPoint™ incorporates custom validation rules for each data point and a robust query monitoring system to manage it all.
Concise Reporting
TrialPoint™ EDC can import data libraries developed in Microsoft Excel to create electronic case report forms and export to CDISC (or other preferred export methodolgy) at end of study. In addition, a wide selection of standard reporting tools and custom templates lets you find the information you need quickly during a study.
TrialPoint™ standard reporting templates include:
- Site enrollment rates
- Subject enrollment rate
- Screening rates
- Follow-up visit compliance rates
- Monitoring rates
- Safety reports
Custom reports are always available and can be built to any sponsors specifications.