iQuality, an efficient Quality Management Software to begin the digital transition to a paperless business operation. In this iQMS webinar series, we shall discuss the interacting elements of a QMS based on the processes and procedures of CAPA and NC and to manage resources and policies collectively to be in compliant with the regulations. For a complete and effective incompliant operation, the life science industries must undergo significant changes to focus on the customer needs and internal efficiency. This is where a quality management system aids an active participation to enhance quality processes and procedures adhering to standard regulations in the interest of public health.
The areas like regulatory needs, auditory functions, data integrity can be managed with an automated quality management system like iQMS. With this, your CAPA’s and NC’s will have an effective investigation process, robust root cause analysis, and corrective actions implementation with a goal of preventing the reoccurrence in future with the potential preventive actions. The metrics and reports of iQMS help the organizations to gauge the management performance review, analyse the risk-based decisions and check the effectiveness of implemented actions.
This Presentation gives a clear view about iQuality Eqms and its features and how it helps in handling CAPA Process
Topics Covered:
- Risk Evaluation
- How to streamline Internal Communication with CAPA Management?
- What about the Rest?
- How I Quality’s iQMS enables you to handle your CAPA process?