Clinical Data Management, simplified
mEDC is a web based electronic data capture system that offers faster study setup, flexible configuration, detailed reporting, improved query management, all leading to enhanced user experience.
- Intuitive user interface
- Quick study setup
- Simpler dashboard & workflow for Sites
- Built-in reports facilitating easier SDV and for RBM projects
- Built-in auto medical coding
- Dynamic CRFs and CRF versioning
- Data exports to SAS, ODM, CDISC, XML and Excel formats
- 24/7 Tech Support
Simplified eCRF creation: An unique interface for stakeholders to design and create complex CRF forms and Edit checks easily.
Highly configurable and adaptable: To accommodate the best practices in clinical trials, and can be easily customized for any specific study phase or therapeutic area.
Run adaptive trials and implement protocol amendments quickly: Sponsors can now deploy all mid-study amendments without compromising study database integrity. mEDC manages multiple CRF editions and seamlessly migrate existing data into new forms and visit structures.
Rich, intuitive user interface: User friendly, easy navigation and rich graphical interface with robust features ensures high acceptance by the stakeholders.
Increased data accuracy and reduced cleaning time: With sophisticated edit check programming and auto medical coding feature.
Seamless integration with third-party systems: Easily shared with other clinical systems like IWRS, IVRS, CTMS, ePRO and drug safety systems.
Lower total cost of ownership: Easy to install and set-up, and requires less programming/technical knowledge. With flexible deployment options and support services, mEDC is best ROI which truly reduces the clients total cost of ownership.
Data Security: Client study data is protected and proper back up is maintained. Our Data Center is SSAE16 and SOC 3 Certified.