RR1 Posted May 3, 2009 Share Posted May 3, 2009 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! Link to comment Share on other sites More sharing options...
RR1 Posted May 4, 2009 Author Share Posted May 4, 2009 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.. Link to comment Share on other sites More sharing options...
scubasammy Posted May 9, 2009 Share Posted May 9, 2009 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 Link to comment Share on other sites More sharing options...
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