Trial Intelligence

Electronic Case Report Form (eCRF)

Capture, manage, and integrate study data while ensuring protocol compliance, and data accuracy and integrity

Dynamic (conditional) Navigation gives you the control you need to collect information based on the responses to other data fields, while providing users with a better experience

Simple Query Management and a rich user interface enables monitors and other staff to easily identify, flag, and resolve data integrity questions

On-page Query Management allows users to review and address all types of queries (protocol deviation, data completeness, etc) within the context of the eCRF and study visit, ensuring protocol compliance, and data cleanliness and accuracy

Real-time Data Validation (edit checks) ensures data integrity and accuracy, saving sponsors and their monitors valuable time while minimizing the need for call-backs

Auto-calculate fields (triggers) reduce data entry burdens by populating data fields based on values submitted in other fields (i.e., calculate age based on date of birth field)

Robust adverse event (AE), serious adverse event (SAE), and ConMed manager enables you to capture, set auto-alerts, and report events and medications that will impact efficacy and safety analysis

PDF support ensures that each page or the entire eCRF can be electronically saved or printed