(Sparta Systems: Holmdel, NJ) -- Sparta Systems Inc. recently announced the availability of TrackWise Clinical Quality Management Solution, providing an end-to-end system that streamlines the oversight of business-critical clinical trial processes and helps ensure compliance with global regulatory standards. This extension of the TrackWise enterprise quality management system (EQMS) drives organizational efficiencies beginning with preclinical activities through manufacturing and post-market operations.

Successful clinical trials are the lifeblood of a life sciences company, with expanding global operations making the effective planning, coordination, collaboration, and oversight of these events a business-critical activity. As companies continue to expand their clinical operations to sites in dozens of countries, completion of these trials has quickly become the longest and most costly stage in the drug development process. This holistic approach for the oversight of quality and regulatory processes moves beyond the more typical subject-centric applications widely used today and helps to prevent costly and time consuming operational quality problems caused by a lack of oversight and control.

TrackWise Clinical Trial Quality Management Solution provides closed-loop process support to allow issues to be reconciled and corrected before they escalate. The solution manages incidents, structured audit programs specifically tailored around clinical trial execution, the associated CAPA and change control processes as well as trial registration and trial documentation/standard operating procedures. With more than 15 years of life sciences expertise, Sparta Systems understands the needs of organizations in this market and has evolved TrackWise software to meet and exceed its customers' clinical quality management requirements.

For more information on TrackWise Clinical Trials Quality Management, visit www.sparta-systems.com/