How are others linking their quality system practices to enable easy tracking of all documents -especially at inspection? (change control/ risk assessments/ validations/ QI)

All tips appreciated!

Just for info to UK staff.........you can see FDA/ CAP deficiencies cited for US labs under 'References'- 'bloopers'.The FDA sub-section has approx 4,400 submissions- together with the blood bank responses. Really interesting stuff..

as per the previous question about capa, a qms will manage from audits through to change management, training management, document control, etc. one system with various workflows and action items see sparta-systems.com if you want to read up on what a qms can do