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 8671I 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.
3414how 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 11625Which of the following Master data is relevant for QM? Vendor Master Customer Master Production Version Q-Info Record
XYZ,
1 2958Post New SAP QM (Quality Management) Questions
How do you manage defects in the material supplied by vendor/supplier?
'could not create return delivery wm movement type 102 not allowed for warehouse no. 010'. How do I fix this problem?
Explain quality management specific data that you can maintain in material master to control the inspection plan?
Which steps must be used in implementing a quality management system?
What is a discovery method?
What do you define in an inspection plan?
How do you get inspection lot certificates?
What are different standard reports in sap quality management system?
What is quality improvement activities?
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
What is the differences between i.s.o and c.m.m levels?
What are quantitative specifications under master inspection characteristics?
What are the most likely quality consequences of choosing an inappropriate life cycle model for a software project?
What does 6 sigma represent?
Which movement types refer to inspection origin 05?