PHILADELPHIA, PA--(Marketwired - Jun 23, 2016) - MasterControl (DIA Booth #1103), a leading global provider of enterprise quality management software (EQMS) and quality consulting services for regulated businesses, will be demonstrating the industry's first Clinical Quality Management System (CQMS) at the DIA 2016 52nd Annual Meeting June 26-30, 2016.
MasterControl's Patricia Santos-Serrao, RAC, Director of Clinical and Regulatory Solutions for the Pharmaceutical Industry, who is life sciences industry expert, will be available for on-site media interviews during the event.
Only MasterControl offers such a breadth of clinical products and solutions, addressing needs for both clinical trial study management and clinical quality management. Because MasterControl's products and solutions are uniquely built to integrate so powerfully, customers can adopt the module that is most needed, such as TMF, then build on this module by adding additional MasterControl products and solutions.
"The role of quality can now take its rightful position as a critical element of a properly managed clinical trial," said Santos-Serrao. "MasterControl is committed to providing technology to streamline and manage the documentation and the high volume of artifacts, activities, and milestones throughout the life of a clinical study. As an example of MasterControl's ongoing innovation tailored to address the needs of clinicians, we will soon introduce the industry's most powerful eTMF solution."
MasterControl CQMS is the most robust system on the market -- designed to manage and seamlessly integrate all documents, activities, project tasks, processes, quality events, relationships, audits and training, all of which must be administered and controlled throughout the life of a clinical trial.
The Drug Information Association 52nd Annual Meeting takes places June 26-30, 2016 at the Pennsylvania Convention Center in Philadelphia. It is the largest global interdisciplinary event that brings together 7,000+ key thought-leaders and innovators from industry, academia, regulatory and government agencies, health, patient and philanthropic organizations from around the globe - and across all disciplines involved in the discovery, development, and life cycle management of health care products.
MasterControl is a committed team of quality, regulatory and software experts who work to empower regulated companies to get their products to market faster. For almost 25 years MasterControl's quality management software solutions (EQMS) have been reducing overall costs, increasing efficiency and accelerating compliance, all creating a significant competitive advantage for customers. Drawing upon unparalleled industry experience, MasterControl offers a suite of seamlessly integrated and scalable software solutions for quality management, document control, product lifecycle management, supplier management, audit management, training management and much more. MasterControl's complete quality management solution is designed for easy implementation, validation and use, continually improving on the promise of "Compliance Accelerated." For more information about MasterControl, visit MasterControl or call 1.800.825.9117 (U.S.); +44 (0) 1256 325 949 (Europe); +81 (03) 5422 6665 (Japan); or +61 (3) 9717 9727 (Australia).