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Serious adverse event
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111	U.S. Department of Health and Human Services MEDWATCH For VOLUNTARY reporting of adverse events, product problems and Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Pharmaceutical industry Clinical research Health MedWatch Adverse event Serious adverse event Medical device Adverse Event Reporting System Medicine Pharmacology Pharmaceutical sciences
112	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
113	COMMONWEALTH OF MASSACHUSETTS DEPARTMENT OF MENTAL HEALTH GUIDELINES FOR THE REPORTING OF ADVERSE INCIDENTS RELATING TO RESEARCH The Department Research Review Committee must implement the following guidelines for the re Add to Reading List Source URL: www.mass.gov Language: English - Date: 2014-07-31 12:15:26 Adverse event Serious adverse event Medicine Clinical research coordinator Pharmaceutical industry Clinical research Research
114	Microsoft Word - guidelines_reporting_adverse_events.doc Add to Reading List Source URL: www.mass.gov Language: English - Date: 2014-07-31 12:15:25 Adverse event Serious adverse event Medicine Clinical research coordinator Pharmaceutical industry Clinical research Research
115	Microsoft Word - serious_adverse_event_report_form.doc Add to Reading List Source URL: www.mass.gov Language: English - Date: 2014-07-31 12:15:26 Data Technology Adverse event Serious adverse event Email Communications protocol Clinical research Pharmaceutical industry Information
116	University of Guelph Research Ethics Board (REB) Event Form Definitions: Add to Reading List Source URL: www.uoguelph.ca Language: English - Date: 2014-10-20 14:49:20 Adverse event Incidental findings Knowledge Business Science Clinical research Pharmaceutical industry Serious adverse event
117	What Is VAERS? vaccine. Rarely, people who have been vaccinated will get unexpected reactions that are serious and should be reported to VAERS. Add to Reading List Source URL: www.state.in.us Language: English - Date: 2014-11-14 18:24:46 Vaccines Medicine Food and Drug Administration Public safety Vaccine Adverse Event Reporting System Vaccine injury Anthrax vaccines Safety Drug safety Prevention
118	COPDGene_AE_Serious_21Feb2008 Add to Reading List Source URL: www.copdgene.org Language: English - Date: 2013-02-18 14:49:16 Adverse event Science Business Knowledge Clinical research Pharmaceutical industry Serious adverse event
119	Docket No. 00N- 1484 13 Oct 2003 Quintiles, Inc. Page 3 of 5 Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-10-28 17:03:10 Clinical research Pharmaceutical industry Pharmacy Food and Drug Administration Quintiles Clinical trial Medical error Pharmacovigilance Serious adverse event Pharmaceutical sciences Pharmacology Research
120	COPDGene_AdverseEvent_4Feb2008 Add to Reading List Source URL: www.copdgene.org Language: English - Date: 2013-02-18 14:47:52 Serious adverse event Adverse event Syncope Medicine San Francisco Syncope Rule Clinical research Pharmaceutical industry Research

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