EasyCDM Suite is a 21 CFR part 11 compliant Electronic Clinical Data Capture (EDC) and Clinical Data Management (CDM) solution that provides powerful and user-friendly environment for clinical data entry and monitoring for clinical trial investigators and trial monitors.
EasyCDM Suite supports all the steps of the clinical trial/research process from clinical trial protocol initiation to data capture and finally clinical data in ready to use format for report and analysis.
It is a web based tool that can be accessed from anywhere in the world by authorized user securely.
Integrated components of EasyCDM Suite:
- Initiation of Protocol →Design of CRF → Setting-up Database → Creation of Dataset.
- Standards Compliant: CDISC Standards (CDASH, SDTM), Sponsor standards.
- Cost Effective & Efficient: Bring the best EDC technology to studies of all sizes.
- All Types of studies can be built in: 100% customizable layout, easing transition from paper to EDC.
- EasyCDM Suite is an easy hybrid system for both electronic and paper studies.
- Available as a SaaS application with subscription-based pricing.
- Robust reporting capabilities including dashboards, standard reports and ad-hoc reports.
- Extensive search and filter options using multi-criteria selections.
- Intuitive role-based and workflow-based views and displays.
- Web services enabling interoperability with third-party applications.
- Minimal learning curve for rapid study start-up.
- Immediate data visibility for all appropriate study stakeholders.
- Run adaptive trials and implement protocol amendments quickly.
- Ability to conduct truly global hybrid (PDE and EDC) clinical trials on one system.
- Easy transition from paper to EDC with minimal training required.
- CRF design closest to paper providing users with an easy to use interface.