Connecting Investigators & Trial Sponsors to Compliance

We deliver industry-leading investigator regulatory solutions for clinical trial sites, sponsors, and CROs

Live Webinar! Thursday, September 22nd at 1:00pm ET
A Journey Through eRegulatory with Coastal Pediatric Associates.

We focus on automating investigator regulatory compliance to enable accelerated study startup and on-demand monitoring, unleashing you to start backlogged trials.

eReg for Research Sites

Whether on-site or remote, our eRegulatory solutions eliminate paper, redundancies, manual processes and site monitoring burden. Through a combination of automated eReg workflows and comprehensive support, we help you start more studies with more investigators faster. Complion’s technology is easy to implement for trial sites, SMOs, IROs, hospitals, health systems and academic medical centers.

Investigator Site Files for Sponsors and CROs

Complion’s eISF (Investigator Site Files) solution enables trial sponsors and CROs to get real-time access to the data required for conducting remote monitoring and decentralized trials. Our remote ISF review functionality accelerates the study startup process while ensuring inspection-readiness with live site monitoring. Leverage ISF Connect to ensure rapid deployment and adoption of the industry’s leading eISF technology for all sites – anytime, anywhere.

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Faster inspection-readiness for sites on trial
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Decrease in monitoring interactions with sites
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ROI in reduced  monitoring and material costs
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Productivity boost  for sites and project teams
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Increased rate  of study starts for sites, sponsors and CROs

Transforming Clinical Trial Site Compliance

Complion enables investigators to be regulatory-compliant on demand in study startup, monitoring, and closeout. By reimaging cumbersome documentation processes with a focus on compliance automation, Complion unleashes sites, sponsors, and CROs to start more trials faster. Complion’s ISF Connect automates regulatory compliance based on the investigator, study and integrated systems to accelerate startup, and increase new study starts.


The number of Investigators currently supported on over 20,000 active eISFs across 50 countries. Complion is the original pioneer of investigator regulatory technology – eReg and eISF, having launched the first-of-its-kind solution more than 10 years ago.

Complion is committed to advancing clinical research through technological innovation and industry thought leadership.

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Ready to get started? Request a Demo

Ready to get started? Request a Demo