Document Revision Management Software

MasterControl Inc.'s Document Revision Management Software System ensures compliance in FDA and ISO regulated environments.

An integral part of any quality management software is a document revision management software system. The revision control system ensures that the right documents and forms are used every time.

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Document Management Resources

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Data Sheet: MasterControl Documents Data Sheet: MasterControl Change Control
Industry Brief: Reducing the Documentation Burden in FDA Design Control Industry Brief: SOP Management as a Compliance Tool in FDA and ISO Environments Industry Brief: How Effective Document Management Helps Pharmaceutical Companies Accelerate Time to Market
White Paper: Automating Document Control Processes to Comply With FDA and ISO Requirements

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Sustain Compliance with MasterControl's Document Revision Management Software System

When an enterprise is spread across multiple locations with a huge number of employees, it is increasingly difficult to manage and control the way operations are completed. Many companies run the risk of non-conformity and non-compliance. These factors may cause the company to fail attaining ISO compliance and lose potential sources of business. The best way to control the execution of processes is to document all the necessary standard operating procedures on one location from where employees can access the specific documents for reference. Usually, companies rely on paper-based or hybrid systems to put everyone on the same page. However, with constant SOP alterations, paper-based systems can become inefficient and cause excessive delays in document approval. At times, the routing and escalating of documentation may cause unnecessary delays and miscommunication between various departments in the company. The solution is to incorporate MasterControl's document revision management software system to eliminate excessive time delays, non-conformity and non-compliance in the way SOPs are executed in the company.

MasterControl's document revision management software is all about providing companies with the competitive advantage of controlling and managing documentation. ISO 9000, 9001 and 14000 clearly stress system transparency through written standard operating procedures and by ensuring that the current manufacturing processes strictly adhere to these documented processes. In a small company, a paper-based system can adequately do the job for a short time. But in the long-run, multiple versions of documents can create difficulty. If an outdated version of a document is used for manufacturing, the company can fail to attain ISO certification, potential capital, customers and a niche in the market. This is why document control is so necessary. MasterControl's document revision management system enables companies to control document revision and maintain updated versions in its web-based repository, accessible to users from virtually anywhere. This means that the required documents are always a click away.

FDA GxP standards require regulated companies to document and track all content and quality processes across an enterprise. MasterControl's document revision management system includes a continuum of applications, which are integrated and easy to use, ensuring that the system can be deployed sooner and compliance achieved faster. Each of these applications includes an automatic revision control system. The document revision control system authorizes one user at a time to revise documents, training materials, CAPA forms, and more. The MasterControl suite applications include the following: