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Serious adverse event
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191	ClinicalTrials.gov Webinar Series, March 2011 Overview of ClinicalTrials.gov Deborah A. Zarin, M.D., Director, ClinicalTrials.gov National Library of Medicine I’m Dr. Deborah Zarin, Director of ClinicalTrials.gov and Add to Reading List Source URL: prsinfo.clinicaltrials.gov Language: English - Date: 2014-08-22 16:54:17 Clinical trials Pharmaceutics Pharmacology ClinicalTrials.gov Trials Serious adverse event Approved drug Adverse event Clinical research Pharmaceutical industry Research
192	University of Wisconsin Comprehensive Cancer Center (UWCCC) Data & Safety Monitoring Plan Policy & Procedures Add to Reading List Source URL: cancercenters.cancer.gov Language: English - Date: 2012-04-16 13:47:09 Pharmaceutical sciences Pharmaceutics Clinical research coordinator Clinical trial Safety monitoring Data monitoring committees Adverse event Serious adverse event Food and Drug Administration Clinical research Pharmaceutical industry Research
193	ClinicalTrials.gov Webinar Series, March 2011 Adverse Events Module Rebecca J. Williams, Pharm.D., M.P.H., Assistant Director, ClinicalTrials.gov National Library of Medicine This presentation will be covering the adver Add to Reading List Source URL: prsinfo.clinicaltrials.gov Language: English - Date: 2014-03-11 16:44:02 Research Pharmaceutical sciences Pharmacology Adverse event Serious adverse event Clinical trial International Space Station Clinical research Pharmaceutical industry Spaceflight
194	Report of Serious and Unexpected Adverse Event FORM For any section in which additional space is needed, complete on plain bond paper. Report Type: ____Initial ___ Follow-up ___ Medical Monitor IRB Log No: A- Add to Reading List Source URL: www.uscg.mil Language: English Pharmaceutics Pharmacology Adverse event Pharmaceutical sciences Clinical trial Clinical research coordinator Clinical research Pharmaceutical industry Research
195	REPORT OF SERIOUS AND UNEXPECTED ADVERSE EVENT FORM For any section in which additional space is needed, complete on plain bond paper. Report Type: ____Initial ___ Follow-up ___ Medical Monitor IRB Log No: AStudy Title: Add to Reading List Source URL: www.uscg.mil Language: English Pharmacology Pharmaceutical sciences Pharmaceutics Adverse event Clinical trial Clinical research coordinator Clinical research Pharmaceutical industry Research
196	ClinicalTrials.gov and Related Projects Add to Reading List Source URL: www.lhncbc.nlm.nih.gov Language: English - Date: 2014-08-14 02:58:17 Pharmaceutics Science ClinicalTrials.gov Clinical trials registry Clinical trial Trials Publication bias Adverse event Serious adverse event Pharmaceutical industry Clinical research Research
197	Microsoft PowerPoint - Results Adverse Events ICF[removed]REV.ppt [Compatibility Mode] Add to Reading List Source URL: prsinfo.clinicaltrials.gov Language: English - Date: 2014-03-11 16:44:01 Pharmaceutics Pharmaceutical sciences Serious adverse event Adverse event ClinicalTrials.gov Clinical trial Pharmaceutical industry Clinical research Research
198	Template for Reporting Adverse Events In Human Gene Transfer Trials This template is intended to facilitate the reporting of adverse events in human gene transfer trials. You may download this as a Word document and th Add to Reading List Source URL: osp.od.nih.gov Language: English - Date: 2014-03-21 13:58:18 Medicine Food and Drug Administration Health Nursing research Pharmacology Clinical trial Adverse event National Institutes of Health Serious adverse event Clinical research Pharmaceutical industry Research
199	Use MedWatch to Report Sharps Injuries Q. What is MedWatch? A. MedWatch is a voluntary program of the United States Food and Drug Administration (FDA) for healthcare professionals and consumers to report serious adverse Add to Reading List Source URL: www.sustainablehospitals.org Language: English - Date: 2003-05-19 19:45:15 Health Pharmaceutical sciences Pharmaceutical industry Clinical research MedWatch Adverse effect Serious adverse event Adverse event Medical device Medicine Food and Drug Administration Pharmacology
200	Reviewer Guidance Conducting a Clinical Safety Review of a New Product Application and Preparing a Report on the Review U.S. Department of Health and Human Services Add to Reading List Source URL: www.fda.gov Language: English Health Clinical research Pharmaceutical industry Food and Drug Administration Drug safety Adverse effect Serious adverse event Clinical trial Adverse event Pharmacology Pharmaceutical sciences Medicine

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