<--- Back to Details
| First Page | Document Content | |
|---|---|---|
 Date: 2015-02-13 11:42:34Food and Drug Administration Personal life Personally identifiable information Pharmaceutical industry Pharmacovigilance Adverse event Internet privacy Question Center for Veterinary Medicine Pharmaceutical sciences Pharmacology Clinical research |
Add to Reading List |
FDA - Pharmacovigilance Workflow Manager (P[removed]txt | 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 |