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5 Why is one of the most commonly used root cause analysis methods. Typically, it is done with a manual, paper-based process and remains outside of the EQMS system. However, this manual approach is not very effective because data and findings from the 5 Why process would have to be added manually into the QMS after the investigation; collaboration would have to be done outside the QMS with important files and documents remaining outside. Thus, the data and findings do not roll up to other team members, and siloed data is not very useful.
A manual approach also leads to increased chances of miscommunication and lack of collaboration while planning corrective or preventive actions. Ideally, we need a 5 Why system that is digitally integrated with your organization’s EQMS.
Realizing the benefits of digitizing root cause analysis, ComplianceQuest has introduced the CQ 5 Why Whiteboard which:
The 5 Why Whiteboard can help increase the effectiveness of a CAPA. It also promotes the use of best practices across teams and minimizes variations in how RCA is performed. Documentation can also be standardized.
Some of the key features of ComplianceQuest’s ‘5 Why Root Cause Analysis’ include:
Also, one can download the detailed 5 Why RCA document as a pdf and share it with users who do not have access to the 5 Why Whiteboard such as external regulatory bodies like FDA that might be auditing the system.
If you would like to benefit from this new feature for root cause analysis from ComplianceQuest, contact us now.
From a Quality Management standpoint, a problem may be reported in an organization from one of the following processes:
Since a problem may have its origin elsewhere, drilling down and asking the right questions is not a boardroom activity but requires the people on the shop floor, the quality team, and other stakeholders to get involved. A typical and effective process would include:
Digitally integrating the 5 Why Root Cause Analysis with your EQMS can help in many ways, including:
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