Yes, I have a wicked dream.

Manufacturers spend too much on quality issues. Some issues they are blind to, some are due to poor detection, and some are the costs incurred when issues escape to a customer.

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.

Unpatched vulnerabilities

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.