Many life sciences companies find it advantageous to outsource some of their functions to contract manufacturers, testing laboratories, and research organizations (CxO). This may include the design of a protocol, selection or monitoring of clinical investigations, evaluation of reports, and preparation of materials to be submitted to the Food and Drug Administration (FDA). Outsourcing allows pharmaceutical and medical device companies to concentrate on their core competencies and at the same time reduce labor and overhead costs. In some cases, outsourcing provides access to expertise and facilities that don't exist in-house.
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DoD 5015.02 requires the visibility of documentation via searchable metadata. The MasterControl software system provides highly sophisticated searchability via the InfoCard. Every document is linked to an InfoCard(s) which contains a variety of document-related metadata. These features allow MasterControl users to enjoy advanced search features that reduce the time required to locate essential documentation.
MasterControl's document control system also allows users to collaborate as they edit and route documentation within a secure, centralized system. The system also automates the routing, approval, follow-up and escalation processes.
MasterControl also allows users to search, collaborate and approve documentation from virtually anywhere in the world. The web-based and very secure centralized system allows users to streamline the document control process between company satellites and other approved users. MasterControl also provides document version control and reporting features.
MasterControl's document control system automates the management of documentation audit trails complete with time and data stamps. If users choose to print essential documentation it is watermarked and stamped with the expiration date.
Learn more about MasterControl's DoD 5015.02 compliant document control software solutions by contacting a MasterControl representative.