The Electronic Data Capture tool is a clinical research data management system supporting the full life cycle of clinical studies from study inception through data field/form, definitions/specifications, data entry, query resolution, data transfer, and export, and study close-out. EDC streamlines the conduct of clinical trials while providing for greater visibility of the clinical trial process and simplifying the preparation of reports and publications. EDC is FDA 21 CFR Part 11 compliant.
EDC is currently used by the Walter Reed Army Institute of Research, the United States Army Medical Research Institute for Infectious Diseases, ORA (and ORA collaborators such as the U.S. Department of Veterans Affairs and assorted universities), and the Naval Medical Research Command for both clinical and non-clinical study data.
Features:
- Creation of templates for Common Study Designs
- Reuse of Electronic Case Report Forms
- Informed Consent
- Demographics
- Medical History
- Physical Examinations
- Vital Signs
- Labs
- Adverse Events
- Termination
- Customizable Reports
- Coding with the Medical Dictionary for Regulated Activities
- Coding with the World Health Organization Drug Dictionary
- Adoption of Electronic Data Standards
Training & Demos
- A variety of training options and demos are available for EDC.
- If you would like to schedule a demo or training, or have any questions, please contact us.