MasterControl (DIA Booth #1103), a leading global provider of enterprise quality management software 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.
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.
MasterControl CQMS is the most robust system on the market that is 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 over 7,000 key thought-leaders and innovators from various industries around the globe, across all disciplines involved in the discovery, development and life cycle management of health care products.