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Federal Register. Washington, DC: Office of Disease Prevention and Health Promotion. September 4, 2013;78:54469-54470.
This notice calls for comments on a proposed government plan to research and promote adverse drug event reduction. The process for submitting public comments is now closed.
US Food and Drug Administration. June 24–25, 2010; Marriott Residence Inn, Bethesda, MD.
This session kicks off an FDA initiative to redesign drug labeling in an effort to prevent medication errors and develop policies to support the changes. The opportunity to submit comments based on materials discussed at the session has passed.
Agency for Healthcare Research and Quality. Fed Register. September 2, 2009;74:45457-45458.
This announcement and accompanying Web site provide version 1.0 of the standardized guidelines for health care agencies to voluntarily report patient safety and health care information. Empowered by the Patient Safety and Quality Improvement Act of 2005, AHRQ-funded Patient Safety Organizations will analyze and organize the data.
Federal Register. February 12, 2008;73:8112-8183.
These proposed rules seek to support the implementation of portions of the Patient Safety and Quality Improvement Act of 2005 including how entities are defined as a patient safety organization (PSO) and how PSOs will collect and protect safety incident data. The comment period on the proposed rules is now closed.