What

Data Accessibility

Advance site and research interoperability by leveraging clinical trial protocols to guide structured data collection. 

This approach enhances data accessibility, streamlines processes, and accelerates research timelines, delivering substantial ROI for both sites and sponsors, particularly within electronic data capture systems.

Why

Improve Productivity/Reduce Cost

Increased the productivity of an existing clinical trial data transfer process by decreasing data latency, transcription errors, and queries. It allows for the more efficient use of both sponsor, CRO, and site staff time and effort.

Study start-up is time consuming and streamlining data exchange will improve this.

Benefits

Enhanced Interoperability

• Improved data collection efficiency
• Enhanced data accuracy and reliability
• 1.5x faster than manual process
• Reduces data entry error by 99% 
• Increased user satisfaction
• Strengthened interoperability
• More efficient and reduces effort
• Conversion from paper to electronic standards-based formats establishes a framework for multiple innovations such as AI/ML