Windchill CAPA

Manage corrective / preventive actions to improve product quality

If you’re using industry-proven best practices in your regulated or non-regulated sector – including ISO 9000, Six Sigma, APQP, CMMI and FDA 21 CFR Part 820, you must be able to demonstrate compliance with extensive failure reporting and corrective action / preventive action standards. When failures or issues are encountered, they must be documented, tracked, analyzed for root cause, and corrected or prevented – not just in current products, but in future ones, as well.

Windchill CAPA enables proven best practices and compliance with a wide range of CAPA standards, including those in industries like Medical Devices that require rigorous closed loop processes to control both internal and external quality issues, including the health of the quality management system itself. As an integral Windchill module, Windchill CAPA can utilize core Windchill features such as change management to ensure that different teams throughout the organization are coordinated and involved in correcting and preventing product errors.

Attachments:

File	Description	File size
Windchill CAPA Data Sheet		203 Kb