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Using Digitization to Get Ahead in Medtech
Using Digitization to Get Ahead in Medtech
Contact: Jennifer Hurst, Sr. Director, PR & Content
Phone: 1.801.560.9608
Email: [email protected]
Companies developing cutting-edge medical devices need cutting-edge technology for their business processes. Whether a company focuses on finding new device materials, designing non-invasive monitors, or tackling the regulatory process, medtech is advancing too fast for paper-based processes. In a digital age, companies continuing to use paper-based processes will be left behind. For medtech companies in particular, digitization is taking over, and rightfully so—it’s key to conducting clinical trials, navigating the regulatory gauntlet, getting products to market faster, and tracking adverse events post-market. Many companies have embraced this idea and updated their processes to include software solutions replacing paper-based quality management, manufacturing production records, and regulatory information management. A step in the right direction, but it isn’t enough.
About MasterControl
MasterControl Inc. is a leading provider of cloud-based quality and compliance software for life sciences and other regulated industries. Our mission is the same as that of our customers – to bring life-changing products to more people sooner. The MasterControl Platform helps organizations digitize, automate and connect quality and compliance processes across the regulated product development life cycle. Over 1,000 companies worldwide rely on MasterControl solutions to achieve new levels of operational excellence across product development, clinical trials, regulatory affairs, quality management, supply chain, manufacturing and postmarket surveillance. For more information, visit www.mastercontrol.com.
