The legal requirements surrounding certain industries often change, and the companies involved with those products and services are forced to change their systems in order to keep up. Many of these industries, like biotech and pharmaceutical, face huge amounts of paperwork and recordkeeping in order to maintain regulatory compliance and take their products to market. The MasterControl QMS software was designed to streamline this process.
Regulated environments must produce regular reports that have detailed information on their processes. This means that every department in the company must be working closely together, communicating effectively, and contributing to the company’s productivity goals. This software was designed to produce the necessary reports while minimizing the amount of paperwork.
QMS software that is automated and connects all the departments is an important part of regulated or ISO-compliant companies. The goal is to meet the necessary regulations while reaching sustained customer satisfaction through continual improvements. An integrated approach to these changes allows companies to include CAPA software, change control, internal audits, records, document control and more to build quality into the process rather than leaving the responsibility solely on the QA department.
This solution for total quality management follows important principles and industry best practices to provide results for the clients. It was designed to offer an internal standardization across different departments and ensure open communications between them. It also allows the company to balance the relationship between productivity and quality, so they can provide the necessary reports to the industry regulators and still take their products to market.
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