What are quantitative specifications under master inspection characteristics?
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What is valuation mode in sampling procedure?
What is a sampling scheme?
What do you understand by sampling procedure?
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 do I populate additional entries directly into the tables? Is there any direct way to populate fields in the tables?
What do you understand by actual quality level value aql?
What is meant by risk? How you can avoid the risks?
Quality control is reactive in approach?
What are different valuation parameters, and how sampling plan depend on valuation parameter?
What is the inspection type for in process inspection?
What are the quality principles?
What in your opinion is the role of sqa personnel with respect to inspections or testing?