MasterControl TotalPharma BrochureSource: MasterControl
Managing documents, training, and business processes are nightmares shared by all pharmaceutical and biotech companies. MasterControl TotalPharma™ exchanges the nightmares for a dream of a solution that enables these companies to get their products to market faster and improve compliance at the same time. MasterControl TotalPharma has been specifically designed to help pharmaceutical and biotech companies manage all documents and automate regulatory-related processes and training in a single platform.
R&D Managers (Regulatory, Clinical, and Pre-Clinical):• Can use MasterControl TotalPharma to more efficiently organize, search, and take inventory of various study documents within the centralized, secure MasterControl system. With MasterControl’s automated routing and approval functionality, managers can more easily oversee project teams composed of resources from multiple departments, even when those teams are working on multiple projects at the same time. MasterControl also ensures that correspondence from regulatory agencies, CROs, and suppliers is linked to the appropriate documentation.
R&D Document Authors:• Can author documents easily from compliant templates and not have to worry about reworking them to match the templates. Users of Word 2007 can create, revise, and redline documents without leaving Word using the new MasterControl toolbar. With MasterControl, PDFs with content bookmarks can be automatically created for regulatory submissions as well as document control functions. Since MasterControl is a connected and complete system, authors won’t have to constantly move back and forth between disparate systems (from e-mail to Word and then to the document management system, etc.) in order locate a document, revise it, and then send it on for review or approval—MasterControl allows all such actions to be taken within the same integrated system.