The Short Story
- The Top Level Docs of a QMS, e.g. the QM
- How to subdivide Areas into Process Areas? By defining Key Process Areas in a QMS (acc. ISO15504 for instance). Details about Process Areas.
- Documentation levels: QMS artifacts range from the top-level ones (referred above) to the more detailed ones. How could documentation levels be defined?
- And last but not least: How to define your SDP?
