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.
What is defect rejection ratio (drr) and defect leakage ratio (dlr)?
What activities of controlling is integrated with quality management process?
Differentiate between product quality and process quality?
What is the use of sap quality management system?
Quality control is reactive in approach?
How do you set inspection point in an inspection lot?
What in your opinion is the role of sqa personnel with respect to inspections or testing?
What is the inspection type for in process inspection?
What are the quality principles?
What are different standard reports in sap quality management system?
What is a discovery method?
What is valuation mode in sampling procedure?
What is usage decision again inspection lot?
What are six mandatory quality procedures?
