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 If an outdated version of a document is used for manufacturing, the company can fail to attain ISO certification, potential capital, customers and a niche in the market.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:
- MasterControl Documents
- MasterControl CAPA
- MasterControl Change Control
- MasterControl Training
- MasterControl Nonconformance
- MasterControl Audit
- MasterControl Customer Complaints
- MasterControl Forms
- MasterControl Submissions Gateway
For More Information on Document Revision Management Software Systems
MasterControl offers a robust document revision management software system and other software solutions with the tools and services necessary for successful implementation of regulatory compliance.
MasterControl's Resource Center is a comprehensive site dedicated to providing companies with the information they need to make decisions about compliance. Here, companies can learn more about FDA and ISO regulations, industry current events, and revision control system options.
Contact MasterControl Today about Questions on Document Revision Management Software Systems
When sustaining regulatory compliance, a document revision control software system can help regulated companies effectively manage their document and quality processes. To learn more about MasterControl's document revision control system, contact MasterControl online
or call toll free at 1.800.825.9117 to speak with a representative.