Transform clinical trials with remote access to eSource data and documents — in minutes, not weeks.
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Unparalleled eSource Experience and Expertise
Capture eSource directly at the point of care to improve clinical trial efficiency, data transparency and research quality.
Access eSource data and documents
remotely — minutes after the patient visit —
for real-time monitoring and more
Improve patient engagement with personalized reminders and study information sent directly to participants’ mobile device.
Maximize study efficiency and data quality with the most widely used eSource. From study build to data submission, discover how truly paperless data capture can deliver better, faster, safer clinical trials.
Streamline design, optimize execution.
Start better studies with minimal delay, streamline development and ensure quality by design—at the source. From rigorous forms design to convenient online training, paperless eSource ensures highly efficient execution for improved outcomes.
Quality data faster, from sites and patients.
Capture electronic data directly for real time, remote access. From eSource data to electronic drug supply, Clinical Ink transforms data capture to deliver remote data faster.
Data integrations, streamlined development.
Connect data capture technologies to further streamline development. From medical device data to electronic informed consent, centralize and control your studies with the push of a button.
Real time, remote access to data AND documents.
Access data and documents online in real time for remote monitoring and review. From eSource data to patient engagement insights, secure online access dramatically speeds timelines and improves quality and safety.
Submission-ready datasets, real-time reporting.
Generate datasets in real time for real time reporting. From automatic data transformation/mapping to electronic end of study archives, streamline studies to ensure compliance from start to submit.