Transform clinical study protocols into structured XML files. Outputs CDISC ODM XML files following CDASH standards. Streamline your EDC setup and give your clinical design teams a significant head start.
Submit your clinical study protocol document
Extract visit schedules and identify required forms
Outputs CDISC ODM XML files following CDASH standards
Clinical XML transforms your study setup process, providing significant time savings and compliance benefits for pharmaceutical companies, CROs, and research institutions.
Automate the conversion from protocol documents to structured XML, giving clinical design teams a significant head start on study setup.
Outputs CDISC ODM XML files following CDASH standards, ensuring compatibility with regulatory requirements and industry best practices.
Eliminate manual data entry errors and streamline the transition from protocol to EDC implementation with automated extraction.
Built to meet industry standards and integrate seamlessly with your existing EDC systems.
Follows Clinical Data Interchange Standards Consortium guidelines for industry compliance.
Generates Operational Data Model compliant XML files for seamless EDC integration.
Meets Clinical Data Acquisition Standards Harmonization requirements for data collection.
Unified EDC/CDMS platform integration
Currently optimized for Zelta platform with plans to expand compatibility to additional EDC systems.
Future Compatibility
Support for additional EDC systems coming soon
Transform your clinical study protocols into CDISC ODM XML files following CDASH standards and give your team the head start they need for successful EDC implementation.