Tag Archives: GlobalSubmit

Bookmarks – Collapsed or Expanded?

At Cato Research, part of our standard document preparation work for eCTD submission documents is to save every PDF file with the bookmarks collapsed (i.e. only the top level bookmark is visible when the document is opened).  We’re often asked … Continue reading

Posted in eCTD, FDA | Tagged , , , , , , | 5 Comments

GlobalSubmit Suite 2010 Beta Test

GlobalSubmit is hard at work on the next version of their software suite.  In addition to several improvements to both REVIEW™ and VALIDATE™, the next update will also include PUBLISH™, their long anticipated eCTD and RPS publishing tool.  As I’ve … Continue reading

Posted in eCTD, Industry News | Tagged , , , , , , , | 2 Comments

DIA’s 46th Annual Meeting

The DIA Annual Meeting is one of the premier events for professionals involved in the discovery, development, and lifecycle management of pharmaceuticals, medical devices, and related products. With 25 content-area tracks, 330 sessions and 20 tutorials, presentations are geared to … Continue reading

Posted in Conferences and Meetings | Tagged , | 1 Comment

Advice for Sponsors New to eCTD

Recently, GlobalSubmit‘s Kathie Clark took an opportunity to sit down with Cato‘s Director of Regulatory Operations, Evan Richardson, and talk about Cato’s experience with sponsors who are new to eCTD submissions.  Kathie published her interview with Evan this morning in … Continue reading

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Download the Slides from the Authoring Best Practices Webinar

The slides from last Thursday’s webinar with GlobalSubmit on Document Authoring Best Practices for eCTD Submissions are available for download here (PDF file). Thanks to all of you who attended the webinar.  As always, we had a great group in … Continue reading

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