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, subject-reported outcomes, 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 product availability by recording inventory receipts, dispensing and returns, and reconcile with ease
Store study e-binders online – not in filing cabinets – for easy sharing and quick access
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Seamlessly integrate lab results from IDEXX with your study database, avoiding transcription errors
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Collect data and observations from pet parents using our electronic owner diary, ePRO, on their mobile device
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Quickly translate adverse events and concomitant medications into predefined codes, terms, and definitions
Prelude supports the VeDDRA, ATCvet, and VCOG-CTCAE v2 dictionaries
Integrate with VetMetrica to collect, measure, and view health-related quality of life (HRQL) scores in your study
Accurately capture PK data – dosing and sampling time – with one click
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Expedite data capture by entering animal subject data at the group level (e.g., barn or cage) to push to the individual animals’ eCRFs
