MasterControl eDHR™ Toolkit for Medical Device Firms

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Toolkit 1 Videos 1 MasterControl eDHR™ Toolkit for Medical Device Firms Paper-based device history record (DHR) systems expose medical device manufacturers to inefficient processes, poor data tracking, and inaccurate or missing information. As a result of this slow, cumbersome way of managing DHRs and other production records, manufacturers often are unable to ship products quickly with full confidence in quality. MasterControl prepared this toolkit to help address the challenges most medical device manufacturers experience during the DHR process when they aren't properly leveraging an electronic DHR (eDHR) system. These free videos, product data sheets, and white papers cover a range of DHR and manufacturing issues that medical device companies face. How a Med Dev Company Automates eDHR Training ReliantHeart, a manufacturer of advanced mechanical circulatory assist technologies, has leveraged MasterControl to automate its DHR processes and prompts for all related training, including enforced employee training on the production floor. Med Device Manufacturer Relies on MasterControl for More Efficient Regulatory Processes Kerr, a manufacturer of Class I and Class II dental products located in Switzerland, streamlined its regulatory processes and improved efficiency with the help of MasterControl. Megadyne Executive Perspective: Increasing Efficiency for Greater Competitive Advantage Megadyne, a manufacturer of electrosurgical medical devices, touts better control of its audits and increased focus on its core business, thanks to MasterControl.

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