In the stringently regulated FDA environment, regulatory compliance is key to any company's success. Software for enterprise document management from MasterControl offers document management software that is centralized and web-based to ensure compliance, integration, and all the solutions necessary to the many processes that must take place within a large enterprise.
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Companies around the globe have gradually understood the underlying concepts behind success. In recent times, FDA regulations and ISO guidelines have defined the framework for companies in doing business the right way. FDA has devised certain sets of rules for companies of different industries that delineate the structure on which business processes are mapped. Enterprise document management is a concept that is derived to give companies an outline on performing business in a controlled environment. To manage scores of documents pertaining to standard operating procedures, HR policies, marketing brochures etc, companies have incorporated quality management systems that electronically store all kinds of documentation in a virtual platform. This web-based repository helps authorized employees of the company to work together in collaboration. The common exchange of ideas is an inventive tool in bridging gaps between employees that are separated in location from each other. The most important factor is to help employees build documents in any kind of document format or software. MasterControl Documents™ provides enterprise document management that is specifically designed to address all of the FDA regulations as stated in various clauses for industries.
MasterControl’s enterprise document management solution is a complete software offering for managing and controlling all documentation concerns for any company. The process of documenting, routing, escalation and approval is made easy by allowing concerned personnel to edit documents and send them for approval. If a reviewer is unavailable for reviewing, the document is escalated to the next reviewer in line which helps in saving time and ensuring that the documents are approved without any excessive delay. The reviewing process is further enhanced by tracking the changes made to the document. This helps the reviewer speed up the reviewing process by only going through the tracked changes in the document.
Enterprise document management is a fundamental component of any FDA compliance effort. Although essential, regulatory compliance has its challenges. MasterControl Documents offers functionality for effective document revision control and electronic signatures that meet all US federal and other global regulatory environments.
The complete approach for enterprise document management, the MasterControl suite, includes applications that address processes for employee training, change control, audit management, complaints handling, and more.
To learn more about MasterControl and the enterprise document management software that we offer, please feel free to contact a MasterControl representative.