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Adverse event
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#	Item
921	DOC Document Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:41 Medical technology Global Harmonization Task Force Clinical research Pharmaceutical industry Adverse event Eucomed Medical device Medical equipment Medicine Technology
922	PATIENT CASE AUDIT WORKSHEET Clinical Trials Monitoring Branch (CTMB) Cancer Therapy Evaluation Program (CTEP) Division of Cancer Treatment and Diagnosis (DCTD) Add to Reading List Source URL: ctep.cancer.gov Language: English - Date: 2014-03-12 09:53:07 Science Pharmaceutical sciences Design of experiments Epidemiology Medical ethics Clinical trial Informed consent Adverse event Clinical research Pharmaceutical industry Research
923	Form Approved: OMB No[removed]Expiration Date: [removed]DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Center for Veterinary Medicine Add to Reading List Source URL: www.fda.gov. Language: English Pharmaceutical industry Clinical research Research Adverse event Food and Drug Administration Norfloxacin Pharmaceutical sciences Pharmacology Piperazines
924	GHTF SG2(PD) N87R7XML schema for the electronic transfer of adverse event data Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:53 Medicine Global Harmonization Task Force Medical device XML Schema XML Adverse event Medical equipment Computing Technology
925	Improving Patient Safety by Reporting Problems with Medical Devices Medical Product Safety Network Add to Reading List Source URL: www.fda.gov Language: English Patient safety Error Safety Medical technology Medical error Medical device Adverse event Use error Food and Drug Administration Medicine Health Medical equipment
926	JOURNAL OF WOMEN’S HEALTH Volume 16, Number 6, 2007 © Mary Ann Liebert, Inc. DOI: [removed]jwh[removed]Special Report Add to Reading List Source URL: www.fda.gov Language: English Piperazines Cardiac electrophysiology QT interval Adverse Event Reporting System Torsades de pointes Breast implant Norfloxacin Clinical research Approved drug Medicine Health Food and Drug Administration
927	GHTF SG2 Meeting Minutes - October 2000 Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-13 17:52:41 Global Harmonization Task Force Health Medical device Adverse event Report Food and Drug Administration Medicine Medical equipment Technology
928	Please revise the numbers (highlighted) and the percentages using these two numbers as the denominator in Table 4 Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Research Pharmaceutical industry Medical terms Food and Drug Administration Adverse effect Clinical trial Adverse event Placebo Medicine Health Clinical research
929	Commonwealth of Massachusetts Department of Mental Health Central Office Research Review Committee Serious Adverse Event Report Form Add to Reading List Source URL: www.mass.gov Language: English - Date: 2014-07-31 12:15:25 Data Technology Adverse event Serious adverse event Email Communications protocol Clinical research Pharmaceutical industry Information
930	Instructions for Submitting Individual Case Safety Reports to FDA/CVM Add to Reading List Source URL: www.fda.gov. Language: English Pharmaceutical industry Medicine Food and Drug Administration Medical informatics Center for Veterinary Medicine United States Department of Health and Human Services CVM Health Level 7 Adverse event Clinical research Health Research

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