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Serious adverse event
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71	Serious Adverse Event Report Form Add to Reading List Source URL: www.khpcto.co.uk Language: English - Date: 2012-11-26 10:34:17 Health Pharmaceutics Pharmacology Design of experiments Epidemiology Serious adverse event Clinical trial EudraCT Adverse effect Clinical research Pharmaceutical industry Research
72	DOC Document Add to Reading List Source URL: en.horizonnb.ca Language: English - Date: 2011-10-19 11:08:03 Science Pharmaceutics Clinical research coordinator Adverse event Clinical trial Serious adverse event Institutional review board Research ethics Clinical research Pharmaceutical industry Research
73	Microsoft Word - CRF Summary of Changes Version 4, [removed]doc Add to Reading List Source URL: www.pecarn.org Language: English - Date: 2011-10-26 18:57:51 Pharmaceutical industry Research Adverse event Serious adverse event Bronchiolitis Adverse effect Case report form Medical record Medicine Health Clinical research
74	HEADS OF AGENCIES WORKING GROUP ON EUROPEAN RISK MANAGEMENT STRATEGY Add to Reading List Source URL: www.hma.eu Language: English - Date: 2006-12-28 03:18:02 Medicine Clinical research Drug safety Pharmaceuticals policy Pharmacy Pharmacovigilance EudraVigilance Serious adverse event Adverse effect Pharmacology Health Pharmaceutical sciences
75	Addendum to Pharmacovigilance Review Memorandum Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmacology Adverse event Clinical trial Pharmacovigilance Serious adverse event Infusion pump Pharmaceutical sciences Clinical research Pharmaceutical industry
76	FACT SHEET: Never Events Leapfrog Hospital Survey Definition of Never Event In 2011, the National Quality Forum released a revised list of 29 events that they termed “serious Add to Reading List Source URL: leapfroghospitalsurvey.org Language: English - Date: 2014-05-22 08:07:01 Patient safety Healthcare Patient safety organization Never events Medical error Adverse event Pay for performance Computerized physician order entry Medicine Health Medical terms
77	Brenda J. Rose, Pharm. D. Office of Special Health Issues Food and Drug Administration October 20, 2011 Add to Reading List Source URL: www.fda.gov Language: English MedWatch Clinical research Medicinal chemistry Adverse Event Reporting System Serious adverse event Pharmacology Food and Drug Administration Pharmaceutical sciences
78	Adverse Event Data Preparation Checklist Add to Reading List Source URL: prsinfo.clinicaltrials.gov Language: English - Date: 2014-11-17 12:05:43 Serious adverse event Science Business Knowledge Clinical research Pharmaceutical industry Adverse event
79	UNITED STATES OF AMERICAPRIVATE FOOD & DRUG ADMINISTRATION Add to Reading List Source URL: www.fda.gov Language: English Drug safety Pharmaceutical industry Food and Drug Administration Pharmacy MedWatch Pharmacovigilance Package insert The Organ Serious adverse event Pharmaceutical sciences Pharmacology Medicine
80	Designing Adverse Event Forms for Real-World Reporting: Participatory Research in Uganda Emma C. Davies1.", Clare I. R. Chandler2.", Simeon H. S. Innocent3, Charles Kalumuna4, Dianne J. Terlouw1, David G. Lalloo1, Sarah Add to Reading List Source URL: covab.mak.ac.ug Language: English* - Date: 2013-07-08 08:46:48 Health Medicine Pharmaceutical industry Pharmacovigilance Adverse event Serious adverse event European Medicines Agency Suspected Adverse Reaction Surveillance Scheme Clinical trial Pharmacology Pharmaceutical sciences Clinical research

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