Auditors consider such nonconformities as a part of a system failure or its inability to ensure process and product control. It refers to the situation where one of the components of QMS or entire QMS breakdowns or the quality processes fails to address the key requirements specified by a regulatory authority such as ISO 9001. It can be broadly classified as Major and Minor Nonconformance Major Nonconformance It could be a deviation in a process, design, documentation, or procedure that may deteriorate the product quality. It generally refers to a product/material that doesn’t conform to the specifications defined/customer requirements. Let’s quickly have a look through the basic definitions for Nonconformance and Noncompliance before diving deep into the details Nonconformance But once you will get to know how these processes work for attaining the goal of product quality, there won’t be a room for confusions anymore.ĭefining Nonconformance and Noncompliance In this post, we will understand the differences between the two, which may initially seem trivial to you. Since both the terms are used interchangeably, the confusion is the common outcome. Do you often feel confused with the usage of terms Nonconformance and Noncompliance? If yes, you are not alone.
0 Comments
Leave a Reply. |