Tag Archives: best practices

Slides from “Planning for FDA Clinical Site Inspections” Webinar

Posted on 29 April 2010 by EvanRichardson

Earlier today, Cato Research Regulatory Scientist Cathy Anderson hosted a webinar titled, “Planning for FDA Clinical Site Inspections: Are You at Risk?”  Those who attended got some great practical advice, along with some real world examples of what can go … Continue reading →

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Advice for Sponsors New to eCTD

Posted on 19 April 2010 by MegWalz

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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Free Webinar – Planning for FDA Clinical Site Inspections

Posted on 16 April 2010 by MegWalz

Join Cato Research for a free educational webinar on Thursday 29 April 2010 at 2PM EST. Cato Research Regulatory Scientist Cathy Anderson will be presenting “Planning for FDA Clinical Site Inspections: Are You at Risk?” Topics covered will include: Responsibilities … Continue reading →

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Advice from the FDA, Part 1: Technical Errors to Avoid in Your eCTD Submissions

Posted on 8 April 2010 by MegWalz

Cato’s Director of Regulatory Operations, Evan Richardson, authored a guest blog post featured on PharmPro.com today.  PharmPro.com is the website for Pharmaceutical Processing magazine, offering a wealth of  information on products, technologies and applications for pharmaceutical and biopharmaceutical professionals. Evan’s … Continue reading →

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Download the Slides from the Authoring Best Practices Webinar

Posted on 29 March 2010 by EvanRichardson

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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