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 7858I 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.
3132how 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 10787Which of the following Master data is relevant for QM? Vendor Master Customer Master Production Version Q-Info Record
XYZ,
1 2132Post New SAP QM (Quality Management) Questions
What is the inspection type for final inspection?
In the region, where there is no quality management, what would you do to introduce the concept of tqm?
Is it possible to cancel the inspection lot once it has been created?
Explain quality management specific data that you can maintain in material master to control the inspection plan?
Quality control is reactive in approach?
What are the different types of defect that can be processed under defect recording?
Which movement types refer to inspection origin 05?
What are quantitative specifications under master inspection characteristics?
What is quality notification?
in the inspection plan I have a characteristic with upper limit. In which table can I find this value?
What in your opinion are the most significant fundamental differences between sei sw-cmm and iso 9000-3?
What is a sampling scheme?
What comes under quality assurance process?
Differentiate between product quality and process quality?
What are the most likely quality consequences of choosing an inappropriate life cycle model for a software project?
