Advice from the FDA, Part 2: Making Your eCTD Submission Reviewer-Friendly

Posted on 14 May 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 post, “Advice from the FDA, Part 2: Making Your eCTD Submission Reviewer-Friendly,” offers practical advice that’s been shared by FDA reviewers at industry conferences over the past year.  In April, the blog also featured Part 1, where Evan discussed some of the most common technical errors found in  eCTD submissions and how to avoid them.

Be sure to stop by PharmPro.com and check out the blog post!

This entry was posted in eCTD, Guest Posts, Publications, Social Media and tagged , , , . Bookmark the permalink.

One Response to Advice from the FDA, Part 2: Making Your eCTD Submission Reviewer-Friendly

  1. Pingback: Tweets that mention Ask Cato » Blog Archive » Advice from the FDA, Part 2: Making Your eCTD Submission Reviewer-Friendly -- Topsy.com