How do states move from discovery to action?
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What are six mandatory quality procedures?
What is quality notification?
What is valuation mode in sampling procedure?
What is a sampling scheme?
What is the difference between GR inspection and source inspection?
What are different valuation parameters, and how sampling plan depend on valuation parameter?
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.
Explain difference between requirement class and requirement type?
How do I use material specification? If I want to use material specification, what are the things I should do?
Explain quality management specific data that you can maintain in material master to control the inspection plan?
Is it possible to make the inspection lot quantity to (1) all the time? Can it be configured as an automatic default in qa01? If yes, what are the steps necessary to make a sample size default every t
How do states move from discovery to action?