What is CoP? CoP is the abbreviation for “Conformity of Production”. But what is it now?
Don’t miss our other articles on CoP-Q and CoP-P. You can also gain in-depth insights in our CoP basic training course.
What is CoP? CoP is the abbreviation for “Conformity of Production”. But what is it now?
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More InformationDon’t miss our other articles on CoP-Q and CoP-P. You can also gain in-depth insights in our CoP basic training course.
“COC” is the abbreviation for “Certificate of Confomity”. The COC document can therefore be translated as “Certificate of Conformity” or “Declaration of Conformity”. Accordingly, the manufacturer confirms in writing with this document that a specific vehicle conforms to an “approved type”. You can find a more detailed explanation in our video. You can find more…
“Product recalls are becoming so expensive thanks to the new Product Safety Regulation that every single one could mean our bankruptcy!” – But is that really the case? Regulation (EU) 2023/988 has been in force since 06/2023 Regulation (EU) 2023/988 (“General Product Safety Regulation – “GSPR”) has been in force since 06/2023 and must be…
The terms approval and authorization are often confused in practice. Although they are related, many people are not aware that the underlying facts are actually different. In our video, we explain what separates the terms and when which usage is correct. Our training courses on the approval process will tell you everything you need to…
A shot about what’s at the beginning of a recall. The most important questions: What is the error? What is the cause of the error? What is the risk – as what can happen to whom with what probability?
As part of the initial assessment, it is necessary to provide evidence of a quality management system (QMS) to the authority. An essential and very important component of a QMS is change management. Basically, it helps the organization to identify and evaluate changes at an early stage. In our video, we explain what change management…
An initial assessment is used to demonstrate the effectiveness of the quality management system to the approval authority.
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