What Should Really Trigger a CAPA?
Corrective and preventive action (CAPA) is often a thorn in the side of medical device manufacturers.
Corrective and preventive action (CAPA) is often a thorn in the side of medical device manufacturers.
Hybrid workspace, societal well-being, and productivity: On the surface, these three concepts aren’t obviously related.
Digital transformation initiatives that aim at getting manufacturers to Industry 4.0 have been around a while and will assuredly continue to be with us for quite a while longer.
"Twins" Credit: Aaure
Today thousands of technologies and solutions help businesses improve efficiency, create better products, evolve faster, and so on.
If there’s anything the last decade has taught us—and the Covid-19 pandemic has punctuated in grand fashion—it’s that businesses must get digital or they may become invisible.
Medical laboratory professionals form the backbone of healthcare and the public health system.
Many tools and concepts can be applied when implementing a transformation in a business. But what makes the transformation meaningful? What is the thing that will drive the transformation’s success?
The 3MF Consortium recently announced its latest volumetric design extension for encoding geometrical shapes and spatially diverse properties through a volume-based description.
This isn’t a new story: A novel technology disrupts society, bringing with it many benefits but also major risks and costs.
The importance of medical device cybersecurity is growing exponentially. As more devices become connected to the internet, threats to public safety mount.
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