Customize the EDC for your research
Visual Study Editor
Build the EDC for your clinical trial yourself in days. No programming.
DICOM & Files
Effortlessly upload any file type and size, and with support for automatic anonymisation of DICOM files.
Explore a suite of features designed to elevate your study's performance.
Build the EDC for your clinical trial yourself in days. No programming.
Effortlessly upload any file type and size, and with support for automatic anonymisation of DICOM files.
Quickly configure complex systems visually, no programming needed.
Configure dynamic rule-based behaviours, such as automatic queries, automatic calculations, conditional field visibility and much more.
Enjoy hassle-free hosting with top-tier AWS infrastructure.
Save time with auto-generated annotated and blank CRFs.
Efficiently manage diverse roles within a single user account.
Tailor field and forms access per user role for precise control.
Create new configuration versions to modify your study and validate the changes in our secure test environment before publishing them.
Full patients automatic update according new EDC settings.
Effortlessly manage different versions, avoiding final reconciliation of data or studying versioning data separately.
Boost data quality with real-time consistency checks, automatic queries, dynamic field hide and much more.
Customise monitoring to achieve approval and review processes tailored to each study.
Ensure timely data entry with automated SMS and email patient and user reminders.
Flexibly export data, choose the format of the exported data, schedule recurring transfers and automate delivery via SFTP.
Streamline data entry by importing information efficiently from CSV files.
ShareCRF helps you meet all regulatory requirements.
Instantly notify staff of key events, ensuring real-time awareness and response.
Insights for effective study management.
ShareCRF is an electronic data capture (EDC) service for collecting and managing multi-site clinical trial and registry data.