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Content-Type: text/plain; format=flowed; charset="iso-8859-1"; reply-type=original Message-ID: <00d601c7503f$23e30230$3454ec04@Diane> Date: Wed, 14 Feb 2007 08:50:48 -0500 Reply-To: Diane <[log in to unmask]> Sender: "caBIG(TM) CTMS Adverse Events Reporting SIG listserv" <[log in to unmask]> From: Diane <[log in to unmask]> Subject: FDA MeetingThought this might be of interest. Diane SENTINEL NETWORK MEETING; PUBLIC MEETING We would like to notify you of an FDA planned public meeting on the development of a virtual, integrated, electronic network - the Sentinel Network. The Sentinel Network would integrate existing and planned efforts to collect, analyze, and disseminate medical product (human drug, biologic, or medical device) safety information to healthcare practitioners and patients at the point-of-care. The public meeting, which will be held on March 7-8, 2007 in Rockville, MD, will address the current needs in medical product adverse event data collection and analysis, efficient use of information technology, and opportunities for public and private collaborations. Additional information is provided in the Federal Register Notice, http://www.fda.gov/OHRMS/DOCKETS/98fr/07-141.pdf . Written or electronic comments will be accepted until April 5, 2007. Submit electronic comments to http://www.accessdata.fda.gov/scripts/oc/dockets/comments/COMMENTSMain.CFM?EC_DOCUMENT_ID=1388&SUBTYP=CONTINUE&CID=&AGENCY=FDA
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![]() Center for Information Technology National Institutes of Health Bethesda, Maryland 20892 301 594 6248 (v) 301 496 8294 (TDD) Comments and Assistance Accessibility ![]() |