Prelude’s EDC is a web-based software application designed for clinical trial data collection while maintaining regulatory compliance. Prelude’s modules extend the capabilities of our EDC by adding features such as adverse event coding, trial supply management, and electronic informed consent to streamline the clinical trial process.
Configure randomization – with blocks, strata, and blinding – to conform with any protocol and save statisticians’ time
Quickly translate adverse events and concomitant medications into predefined codes, terms, and definitions
Obtain electronic informed consent from study participants
Get sites paid quickly by setting up a fee schedule based on the study schedule of events
Track trial supply by recording receipts, dispensing and returns, and reconcile with ease
Store study e-binders online – not in filing cabinets – for easy sharing and quick access