How eSource Saves Time and Money in Clinical Trials
Going paperless can optimize and standardize your data management workflow
Eliminating paper by collecting clinical trial data with eSource delivers measurable benefits for sponsors, CROs and sites. It’s a simple, affordable tool that can give researchers more control, optimize trials, and:
Improve data quality
Provide real-time monitoring of patient safety
Standardize measurements across geographies
Build your study in days not weeks with our intuitive drag-and-drop builder. Easily deploy mid-study changes.
No programming required! Access extensive form libraries, study templates, and coding dictionaries, and watch your study build itself.
Save up to 75% over traditional electronic data capture. Pay through a subscription based model with no setup fees.
Involved in EDC vendor selection? This is for you.
Anyone involved in EDC vendor selection, whether at a sponsor or CRO or in a consulting capacity, stands to gain from reading this guide. In addition, anyone with little to no familiarity with EDC has a lot to learn.
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