Embedded below please find the slides from a webinar hosted by Frost & Sullivan today entitled The FDA Mandates XML: Maximize Your Investments Through Dynamic Publishing. The webinar was sponsored by Quark and EMC and had participation from PAR, Pfizer, and Frost & Sullivan.
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.
1 response so far ↓
1 Anonymous // Nov 11, 2009 at 2:18 am
Interesting post. Do you have any customers in Pharma domain who have expressed this problem to be solved?
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