From a Mark Logic perspective, the question this begs is: where do you then put all the XML that you will be creating to comply with these FDA regulations and initiatives?
At Mark Logic, we believe it should be stored not in a relational database and not in a content management system, but in an XML server (e.g., MarkLogic Server) which provides for high-performance storage, search, analysis and delivery of XML content.
At one level more sophistication: while we believe you may wish to use a content management system (e.g., EMC/Documentum, Alfresco) to control the creation process for this content when it comes to what Frost & Sullivan calls "dynamic publishing" of that content, that you would want to turn to an XML server, such as MarkLogic.
Here are the slides from the webinar.
Frost & Sullivan Webinar: FDA Mandates XML
View more documents from Dave Kellogg.

1 comments:
Interesting post. Do you have any customers in Pharma domain who have expressed this problem to be solved?
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