Click on the document management white papers that we offer below (Automated Document Control Processes) the importance of an automated document management and document control system to FDA-regulated and ISO-compliant companies. Unfortunately, many companies continue to rely on paper-based and partially electronic document control systems that are plagued by inefficiency and errors that frequently are responsible for FDA-483 citations or ISO nonconformance which are also discussed in MasterControl's document management white papers.
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As the document management white papers show, converting a paper-based document management process to an electronic process helps eliminate common errors that could lead to serious regulatory problems.
MasterControl Documents, an integrated part of the MasterControl quality management suite, meets all requirements addressed in the document management white papers that we offer above. MasterControl Documents automates electronic document management processes in an efficient and cost-effective manner. Other critical requirements addressed by the document management white papers that MasterControl meets are identified below:
In addition, MasterControl's document management white papers explain how our Explorer, similar to Windows Explorer, is an easy-to-use tool that helps users find and access documents quickly. Every department can maintain its own Explorers and documents can be stored in multiple Explorers. System administrators can control and automatically update the documents through a dynamic link in the InfoCard.
For more information about the items discussed in the document management white papers that you can access above, please feel free to contact a MasterControl representative.