Streamline Electronic Data Capture with iMednet 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.
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 – whether it is randomization, trial supply management, adjudication, ePRO, payments or more. With iMednet’s native modules you can easily access broader capabilities. And with iMednet’s API, you can easily integrate with a wide range of other clinical research technologies, including CTMS, eCOA, eTMF, eConsent and more.
Simplify study builds
iMednet EDC for clinical trials 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.
Ensure efficient clinical trial execution
iMednet’s unified, comprehensive EDC for clinical trials platform connects the entire research team to accelerate clinical trial processes. Data managers can 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.
Streamline study build, execution and management
iMednet’s Core EDC Features:
AE Con Med Linking
Monitoring Trip Reports