MainCongressional requests as tracked by the AIMS system including 1) general information requests, 2) constituent related requests, 3) requests for technical assistance on legislation, 4) review and comment on letters produced by OL, 5) letters expressing concerns from Congress, 6) questions for the record related to hearings, 7) briefing requests, and 8) document requests. AIMS tracks formal written letters, as well as verbal requests for information that are conveyed in email from the Office of Legislation (OL). <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> Number055

Oct 200931Nov 200915Dec 200919Jan 201032Feb 201024Mar 201041Apr 201038May 201032Jun 201046Jul 201033Aug 201048Sep 201028055

FY 2011 Total: 363

Oct 201026Nov 201032Dec 201021Jan 201131Feb 201129Mar 201128Apr 201119May 201131Jun 201143Jul 201130Aug 201143Sep 201130

FY 2012 YTD: 93

Oct 201140Nov 201124Dec 201129Jan 2012Feb 2012Mar 2012Apr 2012May 2012Jun 2012Jul 2012Aug 2012Sep 2012http://www.fda.gov/AboutFDA/Transparency/track/ucm206444.htmFDA-TRACK CDER DashboardMainOEP considers a GAO or OIG study to be open when we receive the request from the agency GAO/OIG liaison. OEP considers a GAO or OIG study to be closed when OEP receives notice from the agency GAO/OIG liaison that the final report has been posted, or, if no report is to be posted, the agency liaison notifies OEP that GAO or OIG considers the study to be closed. OEP tracks these notifications in AIMS and also in an internal database. The total number of open studies for a month is equal to the number of ongoing studies plus the number of newly opened studies that month minus the number of studies closed that month.Number055

Oct 200917Nov 200918Dec 200917Jan 201018Feb 201019Mar 201019Apr 201019May 201018Jun 201015Jul 201014Aug 201013Sep 201014055

Oct 201014Nov 201014Dec 201012Jan 201112Feb 201113Mar 201114Apr 201116May 201116Jun 201118Jul 201118Aug 201119Sep 201120

FY 2012 YTD: 63

Oct 201121Nov 201121Dec 201121Jan 2012Feb 2012Mar 2012Apr 2012May 2012Jun 2012Jul 2012Aug 2012Sep 2012MainInternational requests as tracked by the AIMS system including 1) general information requests, 2) teleconference requests, 3) document requests, 4) visit requests, 5) documents for review and comment, 6) information provided by international regulatory counterparts to the FDA (FYI), and 7) FDA requests for information from international regulatory counterparts. AIMS tracks formal written requests as well as verbal and email requests.Number055

Oct 200940Nov 200932Dec 200925Jan 201028Feb 201037Mar 201040Apr 201031May 201024Jun 201045Jul 201049Aug 201043Sep 201039055

FY 2011 Total: 481

Oct 201046Nov 201047Dec 201039Jan 201122Feb 201121Mar 201117Apr 201143May 201134Jun 201158Jul 201141Aug 201146Sep 201167

FY 2012 YTD: 155

Oct 201151Nov 201158Dec 201146Jan 2012Feb 2012Mar 2012Apr 2012May 2012Jun 2012Jul 2012Aug 2012Sep 2012