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This web page regulatoryone.com states the following, "Sunday, 3 March 2013." Our analyzers viewed that the webpage also said " History and background of GDUFA." The Website also said " The one hundred twelfth congress of the United States of America at the second session on 3. His act may be cited as the Food and Drug Administration Safety and Innovation Act. The amendment is referred to as Generic Drug User Fee Amendments of 2012 GDUFA. What is GDUFA and why was it implemented by FDA? The money ear." The website's header had Drug Regulatory Affairs as the most important search term. It is followed by New Drug Application, Abbreviated New Drug Application, and Certificate of Suitability which isn't as highly ranked as Drug Regulatory Affairs. The next words they used was Drug Master Files. FDA regulations and requirements was included but might not be seen by search engines.