Regulated companies are increasingly recognizing the benefits of employing corrective action software systems and integrating them with process and event management software for better management of document control, change control, employee training, and other processes.
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The main intent of any CAPA program is to correct issues and prevent their recurrence in the system. Companies across the globe are focusing on incorporating corrective action software systems with their quality assurance applications so that issues are easily identified and resolved without any delay. MasterControl offers a corrective action software system that is completely web-based, increases team participation, and involves appropriate employees in the CAPA process. All corrective action-related documentation is available online only to authenticated users. The MasterControl corrective action software system tracks all corrective actions so that users can trace the steps taken to resolve issues. Since all nonconformities are documented, MasterControl corrective action software enables management to easily identify problems, their root causes, and the actions taken for their resolution. The increased visibility is brought about by the built-in analysis tools that help identify weaknesses and also serve as a basis for implementing the corrective actions.
MasterControl's corrective action software system provides a variety of online reports that help the quality assurance team get a live feed of ongoing activities and allows them to address issues as they arise in real time. The MasterControl corrective action software system is completely compliant with regulations such as ISO 9000, ISO 14000 and 21 CFR Part 11 which makes it easier to resolve issues as well as maintain and sustain compliance with FDA regulations and ISO standards. Management can integrate the corrective action software system with the MasterControl Audits program which allows issues identified through audits to be rectified by automating the CAPA process.
FDA 21 CFR part 11 requires that life science companies ensure the accuracy, reliability, and consistent performance of their electronic systems. ISO certified companies and manufacturers also need corrective action systems to meet best practice guidelines. The corrective action software from MasterControl ensures an accurate and reliable system for corrective action or CAPA processes. It also ensures consistent performance. The solution for CAPA is easy to use, easy to deploy, easy to validate, and easy to maintain. It includes best practice electronic forms for efficient data entry, which eliminates the hassle and potential errors inherent to manual data entry. Since all quality processes are connected, a CAPA can be automatically launched upon identification of an issue.
The MasterControl corrective action software system enables management to develop a product training program that trains resources about the company's processes without excessive spending on outsourcing the training to third party organizations. Management can also provide technical support to different vendors and customers which promises increased customer satisfaction and retention. This improves the overall standing of the company in the market and a steady increase in the company's ROI. MasterControl also employs a unique approach to validation that helps companies attain and sustain compliance in the long run.
Corrective Action Software System processes are central to any GxP system. MasterControl corrective action software ensures the corrective action or CAPA system improves product quality and safety, increases customer satisfaction, and ensures FDA compliance. To learn more about corrective action software contact MasterControl online or call toll free at 1.800.825.9117 to speak with a representative.