(866) 258-2735


The iMednet eClinical 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.

View All

The Electronic Data Capture (EDC) technology offered by Mednet streamlines the process of collecting and managing data in clinical trials. By utilizing this EDC technology, researchers can quickly and accurately collect patient data in real time and eliminate the need for paper-based data collection methods, saving time and reducing the risk of errors.

Mednet’s’ EDC platform, iMednet, is user-friendly, customizable, and can be integrated with other clinical trial software, making it an ideal solution for clinical research teams looking to optimize their data management processes.

As the clinical trials industry rapidly transforms, one thing remains constant – clinical research teams need to find ways to build and execute studies quickly and efficiently, while being able to swiftly adapt to a variety of study designs and changes. In an ever-changing environment with evolving requirements and an increasing number of data sources, it can be challenging. Mednet can help. 

iMednet EDC is part of a comprehensive eClinical platform designed to connect the entire team and accelerate clinical research processes. 

Everything you need, at your fingertips

As the core of its 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. 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. 

Simplify study builds

iMednet EDC includes intelligent build tools designed to allow for powerful functionality to implement unique and complex study designs, without the need for custom or costly programming. Studies can be set-up in a matter of days, not weeks or months. Its highly configurable platform allows for complete flexibility, enabling you meet the demands of increasingly complex and varying study designs. 

Ensure efficient trial execution

Data managers can easily review and manage study data throughout the entire trial. Intuitive dashboards and to do lists make it easy for roles to monitor and prioritize tasks. Additional features help expedite study start-up activities, while real-time data and comprehensive reporting tools enable you to quickly generate required reports.  

Access best-in-class support when you need it

iMednet EDC is designed to be inherently easy-to-use, but Mednet also provides a variety of training options for all of your key stakeholders, from study designers to principal investigators and other site users. If you need more help, we can provide additional training or even build the study for you. Either way, our exceptional, tenured and highly responsive customer success team is always here to help. With a team of knowledgeable professionals with experience working in sponsor, CRO and clinical settings, the Mednet team is well-quipped to effectively support your clinical research projects from start to finish.

Adapt to a variety of study requirements with a highly configurable platform. 

iMednet EDC is exceptionally flexible and configurable, meaning that it can easily accommodate your unique workflows, templates and processes. Features like study replication, reusable forms and highly configurable CRFs help you maximize efficiency, while ensuring compliance. 

Optimize your R&D investment with an accessible, affordable platform for all study types. 

iMednet’s software as a service (SaaS) model, coupled with its comprehensive platform, minimizes upfront fees and dramatically lowers overall costs. The transparent approach makes it an accessible and practical solution for all study types, including Phase I–IV trials, feasibility studies and registries. 

Quick access to a comprehensive suite of 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, DICOM Imaging, eConsent or more.  

iMednet makes it easy. Its comprehensive platform is built with native modules, meaning you can easily access broader capabilities. And, because they are ‘built-in’, it is seamless, meaning you can quickly retrieve accurate, real-time data across the platform at any time.

Mednet’s API also allows clinical research teams to easily integrate with the full eClinical ecosystem, including data lakes, wearables, patient recruitment and eTMF. Contact us to learn more.