NetRegulus, Inc. Announces Advanced Capabilities for Study Software – Enhancements Continue NetRegulus Focus on Study Management and Speed to Market
Denver, CO – August 7, 2006 – NetRegulus®, Inc., an established provider of enterprise compliance software for regulated industries, today announced enhancements to the NetRegulus NetRM™ Study solutions. These enhancements continue NetRegulus’ leadership in delivering innovative study data management and electronic data capture (EDC) solutions that meet the critical needs of Life Science companies while improving ease of management oversight and reducing the time to market for a company’s products. Enhancements to the workflow capabilities include seven new pre-configured study workflows that enable users to easily keep track of tasks and alerts that impact their specific role within a study. The flexibility of the NetRegulus workflow engine allows companies to tailor existing workflows or create additional workflow steps, thereby allowing the solution to be configured to specific business or study needs, without requiring customization. This creates the foundation for study managers to more easily review and report on the study’s progress and for each employee to be aware of their individual tasks. When combined with the powerful ad-hoc reporting engine, a study manager can monitor progress within and across studies, by trial site and by subject.
In addition to these new capabilities, NetRegulus announced a number of other enhancements to its study solution. First among those is an improved dual data entry verification process flow for paper-based studies that includes rapid verification of tabular data. In addition, a specific clarification workflow has been added to support either paper-based or electronic clarifications. This approach ensures that data clarifications are processed efficiently and that dependent processes are not closed until clarifications are completed.
“In total, these new capabilities further improve the ability of our customers to improve the speed to market of their new products,” said Lisa Ensign, Director of Product Management for Study Solutions, of NetRegulus. “Our single, integrated solution supports EDC, paper-based collection or a combination of both, providing emerging growth and very large companies with a powerful choice that meets their current and future data management needs. The NetRegulus solution improves the accuracy of data entered into the system, significantly reduces time spent clarifying data, and provides real-time tracking of all data management processes during the course of a study.”
About NetRegulus, Inc.
Located in Denver, Colorado, NetRegulus is a provider of web-based Enterprise Regulatory Management software that allows life science companies to effectively manage their clinical study and quality data. NetRegulus products allow organizations to manage complex data requirements from clinical trials through regulated post market activities within a single integrated and modular system. NetRegulus products are developed to help life science companies meet ever increasing global regulatory requirements and to improve operational efficiencies, launch products to market faster and proactively identify potential product quality problems. For more information about NetRegulus, telephone +1 888 707 6900, or visit the NetRegulus website at www.netregulus.com.
