What are the different types of defect that can be processed under defect recording?
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What are the quality principles?
What is the difference between GR inspection and source inspection?
Explain quality management specific data that you can maintain in material master to control the inspection plan?
What is sap qm ?
When the final inspection is performed in qm process?
What is an inspection plan in qm process?
What are different search criteria you can use in quality management system?
What is valuation mode in sampling procedure?
what is the difference between selected sets and code groups?
What is meant by risk? How you can avoid the risks?
I am in god softwwrae compnay as SAP QM consultant Domain with Pharma industry, I have got an oppurtunity for creating Computer system Validation Documents in Reputed pharma company . Can any one please help me out to prepare the CSV documents.
How many quality principles are there? Could you name few?