Our Complete EDC-centric eClinical Solution
Optimize your clinical trials with iMednet, a cost-effective clinical data management system, centered around a robust EDC with a full suite of native modules. Designed to also allow easy integrations, the platform enables research teams to meet the rapidly evolving requirements of clinical research, while supporting a wide range of study types and designs. iMednet is highly flexible and intuitive, enabling users to get studies up and running quickly, while ensuring easy onboarding of the entire research team and clinical trials sites. Request more information >
Robust EDC
At the core of our comprehensive eClinical platform, iMednet EDC is uniquely designed to help sponsors and CROs achieve their clinical research goals. Highly flexible, it enables you to build studies quickly, while easily adapting to complex protocols and mid-study changes with ease.
- AE CON MED LINKING
- LAB NORMALS
- MEDICAL CODING
- MONITORING TRIP
REPORTS - REDACTION TOOL
- REPORTING
- TARGETED SDV
Premium Native Modules
Optimize your clinical trials with quick access to a comprehensive suite of native clinical research capabilities while also allowing easy integrations. While iMednet EDC is the cornerstone of the platform, sometimes you need additional capabilities – whether it is randomization, trial supply management, adjudication, ePRO, payments or more.
Flexible API
Mednet makes it easy to export or import clinical trial data. Whether through its Data Import Manager or API, iMednet is designed to efficiently share data with other systems and effectively meet the evolving demands of today’s study designs and requirements. iMednet API allows clinical research teams to easily integrate with the full eClinical ecosystem, including eConsent, data lakes, wearables, patient recruitment, CTMS, eTMF, analytics and more.
- CTMS
- eTMF
- DATA LAKES
- WEARABLES
- PATIENT RECRUITMENT
- ANALYTICS
- AND MORE…
Easily configure and manage your own clinical studies.
iMednet is a comprehensive, EDC-centric eClinical platform built from the ground up with key native modules – such as RTSM, adjudication, ePRO, payments, imaging, and eConsent. Designed to allow easy integrations, the platform enables research teams to meet the rapidly evolving requirements of clinical research, while supporting a wide range of study types and designs – including traditional, hybrid and decentralized trials.
Contact us for an introduction to Mednet's comprehensive EDC-centric eClinical platform with key native modules to support all study types and phases – such as randomization, trial supply management, adjudication, ePRO, payments, DICOM imaging, eConsent and more.
Designed to help you achieve success.
Intelligent Build Tools
Simplified wizards make complex study builds easy.
Data Quality
Form edit checks and other rules ensure accurate data and increase efficiency.
Intuitive Platform
Easy to navigate, monitor jobs and prioritize tasks.
Rapid Site Adoption
Comprehensive feature set makes it easy and quick to onboard and perform site tasks.
Inspired Design
Creative development suite enables complete flexibility in study design.
Competitive Pricing
Native modules, predictable pricing create a cost-efficient solution for all study types.
“Having all of your clinical data, but also your external data, which is important too in a clinical trial – having that together, that really makes a difference.”
Pascal Groenen, Factory CRO