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Papers and Presentations

Be sure to visit our Case Studies page for detailed project descriptions.

 
Faster, Better, Cheaper... Validated?!

The FDA wants your software to work right, and if you're in a regulated environment, they have the force of law behind them. But what do you do when you want to apply modern, "agile" software development methodologies in a validated environment? And how do you get regulatory to believe you when you tell them that it's all going to be ok? More...

 
Bridging the Gap with XML: Understanding eContent Server's XML Limitations

If you're thinking about using Documentum in conjunction with XML, there are some important pros and cons to consider. This brief presentation lays out our experiences in this area (in PDF format).

 
Adobe Acrobat, PDF, and Regulatory Submissions

If you're new to the world of Adobe Acrobat or if you'd like to learn more about how to use PDFs in your regulatory submissions, this brief presentation may help (in PDF format).

 
Disaster Recovery

See what Frank Jacquette had to say on the topic of disaster recovery at a recent meeting of the Main Line Association for Continuing Education (in PDF format).

 
Upgrading Documentum

Still using Documentum 4i or EDMS 98? Read our detailed technical paper on the nuts and bolts of upgrading Documentum (in PDF format).

 
Documentum: Where do we go from here?

"Those who do not learn from history are doomed to repeat it." See what the history of the Documentum product suite can tell us about your choices for the future (in PDF format).

 
A Documentum Primer

Throughout the pharmaceutical and life sciences world Documentum has firmly entrenched itself as the document management heavyweight. But what is it, and what is all this "document management" stuff anyway? Read this article to find out.

 
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