- Why SureClinical
- ECO Apps Bundle
- Products
Our Eclinical Ecosystem components include our Eclinical Applications, our Eclinical Collaboration Platform and our Eclinical Intelligence Suite.
Automate, streamline and accelerate clinical operations and quality with our suite of connected clinical applications for project management, quality, and regulated content management for sponsors, CROs and investigator sites.
Our Eclinical Collaboration Platform connects teams with applications and productivity tools such as trusted office document signing, trusted web meetings, automated workflows, forms and a private team network.
Automatically connect, capture, combine and monitor clinical performance metrics and analytics in a single flexible clinical knowledge repository.
Eclinical Applications for Clinical Operations and Quality
Eclinical Collaboration Platform
Eclinical Intelligence Suite
- Services
- Resources
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- About
SureClinical Products

Innovative Solutions for Health Sciences
Innovation is at the core of our values – providing solutions that save you time, money and enhance quality – and also are easy to use, are easy to learn, and are accessible everywhere from any device.
From our innovative trusted clinician network, our applications for clinical operations, to our Enterprise Collaboration Platform for Health Sciences, we deliver the best user experience, product feature and value in the industry. Find out how Going Digital with SureClinical can help your organization pursue the fastest path to success.

Whitepaper:
Estimate cost savings with SureETMF
Clinical trial cost measurement has never been more important. The clinical trial master file (TMF) has traditionally been paper based, resulting in high labor costs and inefficiencies. This white paper shares operational details about how successful organizations are improving clinical operations ROI by automating manual TMF tasks.
Whitepaper:
Automate with Collaborative Portals
Collaborative clinical trial portals can help improve operational efficiency, enhance quality and reduce time consuming manual processes in labor intensive clinical trials. Download this white paper to learn about the use of task automation, digital signing and collaborative tools for SureClinical's portal and eClinical applications platform.
Whitepaper:
Simplifying Compliance with SureClinical
Adopt best practices to drive success with government regulatory requirements. Learn the details of how SureClinical meets government regulatory requirements FDA 21 CFR Part 11, European EC Annex 11, HIPAA and industry best practices through our global cloud, built in security policies, audit trails, and electronic signing policies.
SureClinical
The Fastest Path to Success
Customers and Users
"Our users, sponsors, and investigators are delighted by SureClinical’s suite of eClinical applications, including SureCTMS, SureETMF, and SureDrive."
Gary ZammitCEO of Clinilabs Drug Development Corporation 
"Of all of the systems I use, SureClinical is the best Clinical Trial Management Software."
Deana DowdCRA Consultant, First Coast Clinical Research
“With SureClinical, we cut our clinical trial project startup time in half. Going digital was not only a significant time saver, but it also enhanced the quality of our data.”
Global CRO 
"With SureClinical eTMF Cloud, internal and external study stakeholders can collaboratively complete, digitally sign and share regulatory and study information in the cloud from mobile or web. This strategic capability allows us to eliminate paper at point of origin, accelerating document completion and enhancing document quality."
Lynda ShelleyExecutive Director of Clinical Operations, Novotech
”With SureClinical, our goals of going digital have been met. We tested and sandboxed many systems before making the decision to go with SureClinical for SureETMF and SureCTMS. Our own client users are passionate about the software and it is incredibly easy to initiate, file and manage documents and trials."
Global CRO