What is sap qm ?
What are qualitative specifications under master inspection charactertics?
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 a sampling scheme?
How do you create an inspection method? An inspection method can be created in one plant can be used in other plant?
What is defect rejection ratio (drr) and defect leakage ratio (dlr)?
How do I transfer the results from one origin to another origin?
What is the differences between i.s.o and c.m.m levels?
What do you define in an inspection plan?
How many partner functions are there in sap ?
Do the discovery methods produce data that informs or serves to improve the policy, management, or operational aspects of the program?
I would like to know where the batch status can be set in sap. We have the stock type q for quality inspection. We would like stock type r for rework and s for blocked. Where can this be set in sap?
What is the difference between inspection method and inspection plan?
What is the use of sap quality management system?
What is the use of sampling type?
