MainPercentage of 505(q) petition responses due in the month, completed by deadlineSection 914 of the Food and Drug Administration Amendments Act added new section 505(q) to the Federal Food, Drug, Cosmetic Act (the Act). Section 505(q) governs certain citizen petitions and petitions for stay of agency action that request that FDA take any form of action related to a pending application submitted under section 505(b)(2) or 505(j) of the Act. Under section 505(q)(1)(F) of the Act, FDA shall take final agency action on a petition subject to section 505(q) not later than 180 days after the date on which the petition is submitted.<br>These measures has been retired as CDER has created new measures for FY13 which align to their four functional areas of 1) Regulatory Review and Drug Safety, 2) Drug Quality and Compliance, 3) Transparency and Public Outreach, and 4) Regulatory Science Research. </b>Percentcolumn0100201001002011No petition responses were due in September 20111002012No petition responses were due in October or December 2011http://www.fda.gov/AboutFDA/Transparency/track/ucm206444.htmFDA-TRACK CDER DashboardMain505(q) petition responses due during the monthNumbercolumn02010020112012