Your advantages:

• Enter your data either centrally (DDE from paper) or decentrally (EDC).
• Let your patients contribute by entering some of the data themselves (e.g., quality of life (QoL) questionnaires or other questionnaires).
• Benefit from the powerful roles and permissions framework (selection of modules and question levels available to users) and configure workflows
• Create and edit reports using the online reporting system
• Define cross-page/cross-visit change checks
• Work with fewer additional systems and use the integrated randomization and logistics module
• Include trial centers from different countries or locations in your study—the CRF is available in the appropriate languages and for all browsers
• Attach binary data such as X-rays to the patient CRF
• Increase the quality of your data by applying a source data verification workflow
• And much more …