Let the use case decide: AI and supervised machine learning for EDC in clinical research
- Take advantage of point-and-click electronic data capture designer and automatic design validation.
- Streamlined coding process enhances accuracy and supports regulatory compliance.
- Manual coding searches reduced by >50% with Medical Coding with AI directly integrated into Zelta’s clinical data management and EDC platform.
- Code patient data with a built-in, machine learning-enabled assistant, to maximize efficiency and reduce errors for EDC in clinical research.
- Use supervised machine learning to streamline the manual process of annotating CRFs with CDASH, allowing for quicker clinical study startup.
Simplify the trial experience: for your teams, sites, and participants
- In-app, KPI-based dashboards and visualizations generate real-time insights to monitor trends, identify bottlenecks, and track other clinical study and dataset metrics.
- Immediate feedback during data entry and clinical data acquisition, including real-time edit checks and auto calculations, reduces queries and delivers first-time right data.
- ODM regulatory compliance means faster data integrations and compliant data outputs for any clinical study.
Built-in optimized workflow solutions
- Eliminate building every cycle/visit combination and take advantage of repeating event groups to streamline your electronic data capture workflow.
- Never forget the basics with EDC system level null and future date checks in place from the start.
- Reduce the time required to design and standardize CRFs, allowing for quicker study startup.
Fewer disruptions from mid-study changes
- Quickly and easily make changes and deploy mid-study updates automatically.
- Reduce site and participant downtime from days or weeks to minutes.
- Built-in error checking helps promote confidence in releasing clinical study amendments.
- <30 minutes for data entry lock to deploy mid-study updates in Zelta’s Electronic Data Capture system.
Customizable clinical data acquisition and management functionality
- Manage local labs at a program level, reducing redundant work and ensuring data quality and accuracy across trials.
- Integrate with third-party solutions, CTMS, RTSM, or CDMS with a built-in point-and-click tool.
- View up-to-the-minute study data and easily navigate to points of interest within the data.
- Interact with discrepancies in real-time and action them directly from the eCRF.
- Achieve profound, comprehensive insights from flexible, responsive, and embedded reporting.
