CAPA, FMEA, and the Process Approach
Corrective action and preventive action (CAPA) is probably the most important process in any quality management system because so much else depends on it.
Corrective action and preventive action (CAPA) is probably the most important process in any quality management system because so much else depends on it.
Few of us today are unaware of the significance of cybersecurity and the threat of cyberattacks on our computers, smartphones, and other devices.
Yup, that’s me in the photo. You’re probably wondering how I ended up hanging under a bridge over the Mississippi River. I’m a certified bridge safety inspector.
Corrective and preventive action (CAPA) is a core function in any quality management system (QMS), and a critical piece in the plan-do-check-act process approach.
Every day, manufacturers rely on a large number of tools, machinery, and infrastructure to produce their goods.
With the threat of contamination from harmful pathogens such as salmonella, listeria, and e.
In the age of mass production, the demand for customization is increasing. Customers prefer products catered to their individual needs and preferences over standard items—albeit at a cost.
Despite the important and ever-increasing role of artificial intelligence in many parts of modern society, there is very little policy or regulation governing the development and use of AI systems in the United States.
Assets are resources owned and used by a company to generate a positive economic benefit. Assets can be physical items, like equipment or furniture, or they can be intangibles like software, patents, or documents.
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