MasterControl Pharma R&D BrochureSource: MasterControl
Even a single day’s delay in getting a product to market can result in the loss of millions of dollars of potential profits. MasterControl Pharma R&D is a utopian software solution that integrates advanced document management with a training component to create an unparalleled system specifically preconfigured for pharmaceutical companies’ document and project management needs.
Development Personnel:- The electronic MasterControl system is secure, efficient, and Web-based, meaning that documents can be revised and approved in a timely manner, even by users across multiple departments or geographical locations. MasterControl automates the routing and approval of document tasks, dramatically reducing the amount of project meeting time that is needlessly consumed signing off on tasks. By providing a secure and centralized repository for crucial documentation the Pharma R&D solution makes it easy to track, store, and approve documents from study sites and investigators as well as manage multiple revisions of protocols and similar documents. MasterControl keeps the entire enterprise connected and makes it possible to more efficiently manage project teams that are made up of resources from multiple departments.
Regulatory Departments:- With MasterControl, regulatory professionals don’t have to waste time searching for current versions of documents or manually inventorying and collecting documents for submissions. Tracking correspondence from regulatory agencies and linking it to appropriate project documentation is quick and easy with MasterControl’s comprehensive document management system. The solution also automatically creates PDFs, appropriately bookmarks documents, and simplifies the preparation of legacy documents for submissions.