C
Chance
ASQ QP August 2011 edition (by Karim Lokas) talks about QMS to concentrate on the product instead of compliance.
"QMS began 20 years ago and since then it has widely deployed all over the world. Yet the number of adverse events – quality failures has increased significantly since 2000 (FDA reports).
This is because traditional compliance-focused QMS was designed to support in achieving regulatory compliance. They were not built to support an enterprise quality process focused on the continuous improvement of products." Any comments on this?
"QMS began 20 years ago and since then it has widely deployed all over the world. Yet the number of adverse events – quality failures has increased significantly since 2000 (FDA reports).
This is because traditional compliance-focused QMS was designed to support in achieving regulatory compliance. They were not built to support an enterprise quality process focused on the continuous improvement of products." Any comments on this?