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Company description

Mednet is a leading healthcare technology company delivering eClinical solutions for the global life sciences community. The company's flagship platform, iMednet, is a highly configurable eClinical suite designed to simplify and shorten study build times, increase efficiency in study execution, and minimize costs throughout the duration of a study. Mednet serves medical device, pharmaceutical, and biotech sponsors as well as CRO partners across more than 100 countries, and has supported thousands of clinical studies over more than 25 years in the industry. Mednet is now part of CRScube, expanding its global capabilities and delivering a more connected eClinical ecosystem to sponsors and CROs worldwide.

The iMednet platform is built around a full suite of native, integrated modules accessible through a single sign-on experience. Mednet's quality and compliance professionals average more than 16 years of tenure, and project managers average more than 13 years, ensuring deep expertise is brought to every engagement. The platform supports studies of all types, sizes, and therapeutic areas, and is recognized for its intuitive design, robust reporting, and responsive customer support — earning an average customer review score of 4.9 out of 5 across more than 84,000 site users globally.

Core Platform Modules

• Electronic Data Capture (EDC): The foundation of the iMednet platform, offering high flexibility and intuitive design to get clinical trials up and running quickly. Features include advanced data review and cleaning functionality, detailed user privilege controls, configurable order-of-operations for data review processes, and role-based to-do lists for easy task identification.
• Randomization & Trial Supply Management (RTSM): Supports a wide range of variance and complexity for patient randomization, and simplifies research product inventory management throughout the trial lifecycle.
• Adjudication: Enables clinical event committee (CEC) adjudication workflows natively within the platform.
• ePRO (Electronic Patient-Reported Outcomes): Captures patient-reported data electronically as part of the integrated eClinical suite.
• eConsent: Supports electronic informed consent processes for study participants.
• Payments: Manages site payment and inventory control workflows directly within the platform.
• DICOM Imaging: Provides DICOM image upload and storage capabilities natively integrated into the platform.
• Decentralized Trials: Supports decentralized and hybrid clinical trial models.
• API Integration: Enables connectivity and data exchange with external systems and third-party tools.
• CTMS (Clinical Trial Management System): Supports clinical trial management activities within the unified platform.
• eTMF (Electronic Trial Master File): Manages trial documentation electronically.
• Pharmacovigilance: Addresses safety data collection and reporting needs.
• RBQM (Risk-Based Quality Management): Supports risk-based approaches to monitoring and quality oversight.

Key Platform Capabilities

• Highly configurable study design and build tools that reduce time to study go-live, with development and UAT environments enabling rapid iteration and updates.
• Intuitive dashboards, reports, and patient record pages that surface key information and action items at a glance for site users, CRAs, and sponsors.
• Full suite of integrated modules under a single sign-on, eliminating the need for multiple disconnected systems.
• Strong data review and cleaning functionality with detailed control over user privileges and workflow sequencing.
• Role-based task management and detailed status reporting to streamline data management operations.
• Flexible eCRF configuration supporting virtually any study design requirement.
• Extensive reporting capabilities with ease of training for site staff and study teams.

Who Mednet Serves

• Research Sponsors: Pharmaceutical, biotech, and medical device companies of all sizes, from startups to large established organizations, seeking a flexible and cost-effective eClinical platform.
• CRO Partners: Contract research organizations that require a reliable, scalable eClinical partner with concierge-level service and tools to grow and expand their business.
• Organizations operating globally, with reach across 100+ countries and support for studies in every major therapeutic area.

Company Highlights & Partnerships

• Over 25 years of experience advancing clinical research and electronic data capture.
• More than 84,000 site users and a global footprint spanning 100+ countries.
• Average customer review score of 4.9 out of 5, with consistent recognition for ease of use, customer support responsiveness, and platform versatility.
• Strategic partnership and integration with CRScube, Mednet's parent company, providing deeper regional expertise, scalable support, and a more connected eClinical ecosystem.
• Committed to long-term customer success, stability, and continuous platform improvement regardless of customer size or complexity.
• Leadership team with deep roots in clinical research, healthcare technology, and data management, including co-founder and CEO Rob Robertson and VP of Operations Marci Mogg, who brings over 15 years of clinical research experience.

Mednet's mission is to provide the most innovative, efficient, and effective eClinical solutions to accelerate clinical development, enabling life sciences customers to focus on what matters most — improving healthcare for people worldwide. With its expanded capabilities through CRScube and a proven track record across thousands of global studies, iMednet continues to be a trusted eClinical partner for sponsors and CROs seeking a comprehensive, configurable, and cost-effective platform.

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Software attributed to Mednet

• iMednet EDCView
• iMednet AdjudicationView
• iMednet ePROView
• iMednet PaymentsView
• iMednet DICOM ImagingView
• iMednet eConsentView
• Pharmacovigilance & Safety ReportingView
• iMednet APIView

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