A Robust EDC-Centric eClinical Platform for All Study Types and Phases
The iMednet platform offers a cost-effective solution with a full suite of native tools to simplify and shorten study build times, increase efficiency in study execution, and minimize costs through the duration of the study. For over 23 years, research sponsors and CROs around the world have trusted Mednet to deliver the technology innovation, experience and reliability they need for success.
Contact us for an introduction to iMednet and to discuss your clinical research goals.
Easily configure and manage your own clinical studies
iMednet is a comprehensive, cloud-based, eClinical platform, centered around a robust EDC and built from the ground up with key native modules. Designed to allow easy integrations, the eClinical platform enables research teams to meet the rapidly evolving requirements of clinical research. iMednet is highly flexible and intuitive, enabling users to get clinical trials up and running quickly.
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, and payments. 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.
Everything you need, at your fingertips.
Electronic Data Capture (EDC)
At the core of our platform, iMednet EDC is highly flexible and intuitive, enabling users to get clinical trials up and running quickly.
Randomization
iMednet Randomization supports a wide range of variance and complexity, making it quick and easy to randomize patients.
Trial Supply Management
iMednet makes it easy to manage research product inventory, including auto assignments, auto resupply, manual requests, shipments, tracking and reporting.
Payments
iMednet Payments enables research teams to easily set up robust, customizable payment triggers across an entire study ̶ improving efficiency, visibility and site satisfaction.
ePRO
iMednet ePRO, optimized for mobile devices, allows subjects or coordinators to intuitively enter study-related information, and is accessible – anytime, anywhere.
Adjudication
The iMednet Adjudication module provides complete visibility and is highly flexible, enabling you to adapt any adjudication workflow.
eCONSENT
iMednet eConsent ensures a secure, simple and efficient electronic informed consent process for study participants and site users – supporting traditional, hybrid and decentralized trials.
API INTEGRATION
iMednet’s API allows clinical research teams to easily integrate with the full eClinical ecosystem, including eConsent, CTMS, eTMF, data lakes, wearables, patient recruitment, and more.
Dicom Imaging
The new Imaging module is designed to provide a simple, cost-effective, and secure approach to upload, store and review medical imaging in iMednet, with direct links to the DICOM viewer.
Contact us for an introduction to Mednet’s comprehensive EDC-centric eClinical platform and key native modules – such as randomization, trial supply management, adjudication, ePRO, payments, DICOM Imaging, eConsent and more.
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.
Everything you need, at your fingertips
Seamlessly connected to a comprehensive set of native tools and modules, you are able to quickly and easily leverage broader capabilities to satisfy varying study requirements and needs. And with iMednet’s API, you can easily integrate with the full eClinical ecosystem including data lakes, wearables, patient recruitment, CTMS, and eTMF.
Simplify study builds
Ensure efficient clinical trial execution
Easily capture, clean and manage study data throughout the entire trial. Intuitive dashboards and to-do lists make it easy for key roles to monitor and/or prioritize tasks. Additional features help expedite site start-up activities, while real-time data and comprehensive reporting tools enable you to quickly generate required reports.
Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for over 23 years to deliver the technology innovation, experience and reliability they need for success.
Biotechnology
Pharmaceutical
Medical Device
