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Since your firm (Stratagene) is subject to FDA audit, it already has an
established quality system that probably includes a detailed document review
process. Instead of developing a new process, why not unearth the existing
one?
Dan Goldstein
> -----Original Message-----
> From: Sara Hassen
> Sent: Wednesday, March 02, 2005 11:49 AM
> To: TECHWR-L
> Subject: Document Review Process
>
> Good Morning,
>
> I am trying to develop a document review process for my division. I am
> the lone Technical Writer within a group of scientists (Ph.D. level).
> It is the common assumption that every document I produce should be 100%
> error free. This of course is a daunting task. I strive to maintain
> accuracy, but without a review process, the errors are unnoticed until
> the document is utilized. I proof all my documents twice prior to
> release, but this is obviously not adequate. This brings me to the
> conclusion that a formal review process needs to be implemented.
>
> My question to you is this, how many reviews do your documents undergo
> prior to being released for use? Also, who are the people who review
> the documents, end-users, fellow writers?
>
> I appreciate any and all comments. I am at my wits end trying to
> articulate the need for document review PRIOR to release. I
> am hopeful the information I learn from all of you will assist me.
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