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| First Page | Document Content | |
|---|---|---|
 Date: 2012-11-13 17:52:50Clinical research Medical equipment Pharmaceutical industry Global Harmonization Task Force Adverse event Medical device Patient safety Use error Artificial cardiac pacemaker Medicine Technology Health |
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GHTF SG2 - Global Guidance for Adverse Event Reporting | Print Form Alabama Board of Medical Examiners P.O. Box 946, Montgomery, ALOffice-Based Surgery Adverse Event Report FormDocID: 1vm7X - View Document |
| Washington University in St. Louis Institutional Biological & Chemical Safety Committee Policy on Severe Adverse Event Reporting for Human Gene Therapy Trials As outlined in Section IV-B-2-b-(1) of the NIH Guidelines forDocID: 1vily - View Document |
| National Action Plan for Adverse Drug Event PreventionDocID: 1v1KN - View Document |
| Microsoft Word - FINAL-Formatted-University Adverse Weather and Emergency Event Policy -effDocID: 1uZd2 - View Document |
| National Action Plan for Adverse Drug Event PreventionDocID: 1uxaR - View Document |