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Subject: RE: Extend Enterprise Business Documents toward Pharma?
Gabor, So have you see specializations
of DITA there that would be of value to Pharmaceutical/Regulatory documents, or
things that would be a problem? Joel ----
From: Gabor Fari
[mailto:Gabor.Fari@microsoft.com] I have been very aware of this
working group for years, and have been speaking to the co-chairs, Ann Rockley
and Mike Boses about cross-pollination of efforts. Mike is actually on the
PC-SC as well. -
Gabor From: Joel Finkle
[mailto:Joel.Finkle@imagesolutions.com] I just stumbled upon another DITA subcommittee's
documentation, that of Enterprise Business Documents. There's a great
presentation at http://www.oasis-open.org/committees/download.php/36620/Business%20Content%20Metamodel-1.pptx The document types they're working on are certainly
different from regulatory submission documents, for the most part, but I can
see that a company that already has its HR documents, policies and procedures,
etc. built on this should be able to start extending into regulatory
documentation. This may help us frame the kinds of extensions to the DITA
model that we will need for things such as protocols, reports, etc. On the other hand, this may steer us into thinking in terms
of extension to their data types (Event and Governance, for instance, sound
useful) but might be dead ends in terms of creating our kinds of documents. At
its worst, companies might say that you can't build a DITA-based protocol
without having DITA-based SOPs, DITA-based Policies, etc. etc. which could slow
down acceptance. In any case, it's worth a read. Joel ----
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