http://disqus.com/by/tgpham77/enThu, 17 Sep 2009 17:22:12 -0000http://openregs.com/regulations/view/99189#comment-16836749<p>It is a good idea to data submit and process adverse event reports electronically to help the FDA (Food and Drug Administration) to have quicker access to the reports and to quickly identify and act on the problem(s), it would be safer if the agency also produces and stores hard copies of summaries and processing results of the reports in paper form after receiving and processing them. The electronic system(s) (main and back-up(s)) might be down and might crash which will cause the FDA to lose all data if it doesn't have copies in paper form.</p>tgpham77Thu, 17 Sep 2009 17:22:12 -0000