iMednet EDC

iMednet EDC is a highly flexible and intuitive electronic data capture solution built by Mednet for clinical research teams who need to move faster and smarter. Designed as the core of the iMednet eClinical platform, it enables users to get clinical trials up and running quickly — with no custom coding required — while maintaining the control, compliance, and configurability needed throughout the entire study lifecycle. It is well-suited for research sponsors, CROs, and site teams across pharmaceutical and medical device studies.

The iMednet platform is a unified, comprehensive solution that allows teams to easily capture, clean, and manage study data from start to finish. Its cost-effective pricing model includes unlimited users and sites, making it accessible for studies of all sizes and phases.

Core EDC Capabilities

• Highly flexible and intuitive eCRF design with no custom coding required
• Simplified and shortened study build times with efficient setup
• Intuitive dashboards, patient record pages, and reporting that surface key information and action items at a glance
• Detailed status reporting and role-based to-do lists to easily identify tasks to be completed
• Granular control over user privileges and the ability to set an order of operations for data review processes
• Strong data review and cleaning functionality
• Development and UAT environments enabling rapid updates and mid-study changes
• Single sign-on access across all native modules

Integrated Native Modules

• Randomization & Trial Supply Management (RTSM): Supports a wide range of variance and complexity for patient randomization, plus full inventory management including auto assignments, auto resupply, manual requests, shipments, tracking, and reporting
• Payments: Enables research teams to set up robust, customizable payment triggers across an entire study, improving efficiency, visibility, and site satisfaction
• ePRO: Mobile-optimized solution allowing subjects or coordinators to intuitively enter study-related information anytime, anywhere
• Adjudication: Provides complete visibility and flexibility to adapt any adjudication workflow
• eConsent: Seamlessly integrated electronic consent process that is secure, simple, and efficient for both study participants and site users
• DICOM Imaging: Enables simple, cost-effective, and secure upload, storage, and review of medical imaging directly within iMednet, with direct links to the DICOM viewer
• API Integration: Allows clinical research teams to integrate with a wide range of external technologies including CTMS, eCOA, eTMF, eConsent, and more

Key Platform Advantages

• Seamless access: Real-time, single sign-on access to the full suite of native modules eliminates the need for multiple disconnected systems
• Exceptional support: Partnering with Mednet means access to an experienced and highly responsive support team dedicated to study success
• Cost-effective pricing: Feature-rich platform designed to deliver the functionality of major competitors at a fraction of the cost, with unlimited users and sites included
• Intuitive and configurable: Enables clinical research teams to swiftly adapt to a variety of study designs, complex protocols, and mid-study changes, providing an optimal end-to-end solution for all study types and phases

iMednet is deployed as a unified eClinical platform serving both research sponsors and CRO partners. Its broad module ecosystem — spanning EDC, RTSM, ePRO, eConsent, Adjudication, Payments, DICOM Imaging, and API integration — ensures that all critical clinical trial functions are accessible within a single, compliant environment.