An EHR-to-EDC connector that transfers trial data with accuracy and in just a few clicks.
A faster, more efficient path to clean study data
One of the industry's first EHR-to-EDC connectors, Flatiron Clinical Pipe™ helps create a new trial experience.
Transfer relevant study data quickly and with accuracy, reduce queries, accelerate data cleaning timelines, and hit study milestones faster.
Flatiron Clinical Pipe™ makes a huge difference in getting into the EDC system, period. Regardless of the EDC system we are using.
Dannelle M. Palmer
MBA, PMP, COO, OncoBay Clinical
See how Flatiron Clinical Pipe™ helps you hit study milestones sooner
Flatiron Clinical Pipe™ in action
Outcomes
How Flatiron Clinical Pipe™ supports trial teams
For sponsors and CROs
For clinical trial sites
Get to submission faster while helping your site operate at the top of their license.
Ensure clear data provenance via FHIR logs and an audit trail for all transferred data, assuring confidence in the integrity of the data.
Easily access key metrics sooner to evaluate progress against study milestones.
Save critical time and reduce the need for source data verification on transferred data.
Achieve insight into most reference ranges and data entry date and time, so that pushed data is certified source copy.
Feel confident that your study data is clean, compliant, and protected.
Onboard quickly and easily without needing to learn complicated workflows.
Avoid redundant, frustrating data entry.
Receive fewer data monitoring queries from sponsors.
Reduce the need for source data verification on transferred data as well as the need to obtain and maintain reference ranges.
Transfer data directly from the EHR and avoid manual transcription.
Feel secure in knowing data is encrypted both in transit and at rest.
Learn more about our clinical research product suite
Our clinical research product portfolio reduces burden through technology-supported trials and operational efficiencies, lowers costs and accelerates drug delivery to a diverse patient population, and supports teams from trial design up to FDA submission.
Products and services include:
