So, first, I'm an experienced Sharepoint 2003/2007 IT pro and just love the platform.
I recently have been engaged with a medical device manufacturer who lives and breathes according to FDA regulations and GMP and Quality Management. The environment presently is a mix of XP computers, traditional shared network drives, and a bit of visual
source safe for document storage and control.
While I could espouse how valuable Sharepoint could be to help them regarding their general needs of collaboration, team work, knowledge management, business process management, etc., I'm hoping there may be someone who reads this board and may be able to
express more specifically how Sharepoint can fit in to this FDA regulated environment.
I tried googling to see if there was any success stories of using Sharepoint 2007/2010 in a similar environment such as ISO 9001 or other related medical device manufacturing environment. But I really didn't hit the mark.
So i'm posting this message to see if any of you know of any success stories about how Sharepoint 2010 can be an effective platform in an FDA-regulated, QMS manufacturing environment.
I know Sharepoint could handle much of what we need to do. BUt i'm hoping that I can either 1) obtain a case study showing how some other leading organization adopted Sharepoint 2007/2010 in this ver
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