Author Archives: Meg Walz

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

Posted on 8 April 2010 by Meg Walz

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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Reminder: Free Webinar Tomorrow

Posted on 24 February 2010 by Meg Walz

Last chance to register for tomorrow’s free webinar entitled “Similarities and Differences between CMC Information required for EU IMPD CTA and US IND.” Cato Research Scientist Randy Lane will be presenting and GlobalSubmit‘s Kathie Clark will be available during the Q&A … Continue reading →

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Free Webinar in February

Posted on 12 February 2010 by Meg Walz

Following the success of last month’s event, Cato Research and Global Submit will host another free webinar on Thursday 25 February 2010 from 2-3 pm EST.  Cato Research Scientist Randy Lane will be presenting “Similarities and Differences between CMC Information … Continue reading →

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Upcoming Webinar

Posted on 25 January 2010 by Meg Walz

Cato Research and Global Submit are hosting a free webinar on Thursday 28 January 2010 from 2-3 PM EST, entitled “Effective Project Management Techniques for the Creation of Marketing Applications in eCTD Format.” Want to reduce delays and the need for … Continue reading →

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