SureClinical Launches Eclinical Ecosystem™ ECO Bundle To Support Clinical Trial Automation And Collaboration

Clinical operations ecosystem for Clinical Research Organizations streamlines and accelerates the delivery of new treatments to patients globally

SureClinical, a leading provider of cloud-native eClinical applications, announced the launch of their new Eclinical Ecosystem ECO Applications and Platform Bundle. Designed for the unique needs of Clinical Research Organizations, the ECO Bundle connects people, programs, projects and processes everywhere for a singular view of clinical data. The ECO Bundle centralizes clinical intelligence and reporting across multiple applications, data points and systems, allowing distributed clinical research teams to collaborate within a single, modern, easy to use application experience.

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SureClinical CEO Zack Schmidt brings 20 years of experience in enterprise applications development and product management at leading enterprise software firms Siebel, Oracle and Adobe. With a team comprised of both clinical operations and enterprise software experts, Schmidt and his team are developing innovative technologies that are changing the way clinical trials are managed. SureClinical’s offering connects internal teams and external vendors throughout the entire clinical trial supply chain. The bundle provides the freedom to select and connect the applications of their choice to a single system of record, reduce risk and operational costs, increase efficiency in business reporting, and empower teams with automated solutions to digitize and streamline the clinical trial process.

“Life science clinical operations teams have traditionally struggled to automate business processes. With growing regulatory guidance, recent market conditions, and the impact of the global pandemic, pharmaceutical companies seek digital solutions to connect end-to-end eClinical systems, disparate teams, systems and projects in a timely manner to enhance their treatment quality and reduce business risk,” said Schmidt. “The ECO Bundle answers that need, providing sponsors and CROs with automated tools that are connectable, accessible, extensible and that can be deployed in one day.”

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The ECO bundle supports project management, document management, site management and quality management. With over 500 global clinical trials and multiple audits, and centralized documents and data in one repository, current SureClinical clients have the freedom to select and connect applications from multiple vendors, apps and projects for quantifiable time-efficient delivery of new treatments and therapies. “With SureClinical, we can immediately distribute documents for signature as needed, and we have eliminated our need to manually file documents. Most importantly, we were able to reduce our average site initiation time from 12 months to five months,” said Charity Cowley, Director of Clinical Administration, Applications & Systems.

The ECO bundle includes SureClinical’s SureCTMS, the only clinical trial management system with connectivity to nearly any enterprise application, database or data source, electronic Trial Master File (ETMF), Investigator Site File (ISF), Quality Management Software (QMS) and Clinical Trial Management (CTMS) applications. SureISF is a cloud-based regulatory document management solution for clinical investigators, designed to enable clinical sites to collaboratively view, share, digitally design, comment on and manage site-specific content. SureQMS, designed for global internal and external teams in life science R&D and manufacturing, is a next generation cloud quality management system that unifies, automates and simplifies quality management tasks. SureISF and SureQMS, the newest applications in this offering, are built on SureClinical’s proven ETMF technology; SureQMS offers electronic document, training and quality process and event management that supports the DIA Quality Reference Model.

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