How to Prepare the Functional Requirements Specifications (FRS),If possible please send me the template/format or prepared FRS for Computer System validation in Pharma Industry.
IBM,
1 7451I 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.
2955how to clear inspection stock from qty. one of material is in qty. i am trying using movement type 322 but it is showing error clear inspection stock from qm only. by using qa32 when i am changing status there it is not opening task list tab .any expert can solve thsi problem ?
2 10298Which of the following Master data is relevant for QM? Vendor Master Customer Master Production Version Q-Info Record
XYZ,
1 1678Post New SAP QM (Quality Management) Questions
How many quality principles are there? Could you name few?
What is the use of sampling type?
How to prepare the functional requirements specifications (frs) ?
Explain the different steps that are involved in final inspection process?
Is there a way to create inspection lot programmatically in an abap report? Is there any business object, function module or user exit? We went to 1 lot for 1 shift. We use inspection origin 89 (manua
How do you set inspection point in an inspection lot?
Reduction of scrap increases profitability?
Which movement types refer to inspection origin 05?
Differentiate between product quality and process quality?
What are the different types of defect that can be processed under defect recording?
Where do you use sampling procedures?
What activities of controlling is integrated with quality management process?
What is the difference between good receipts inspection and source inspection?
How do I transfer the results from one origin to another origin?
Explain quality management specific data that you can maintain in material master to control the inspection plan?