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Serious adverse event
Results: 260

#	Item
31	INVESTIGATOR SERIOUS ADVERSE EVENT (SAE) REPORT Add to Reading List Source URL: ranzco.edu Language: English - Date: 2014-06-10 23:41:15 Informed consent Pharmaceutical industry Food and Drug Administration Behavior Clinical research coordinator Medical ethics Clinical research Ethics
32	Social Care Research Ethics Committee Report of significant adverse event (SAE) The chief investigator (CI) should report any SAE that is both related to the research procedures and is unexpected. Send the report to the Add to Reading List Source URL: www.scie.org.uk Language: English - Date: 2014-06-11 04:31:11 Scientific method Science Adverse event Serious adverse event Institutional review board Clinical research Pharmaceutical industry Research
33	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
34	Advisory Note for Using Intracatheter Devices Background The Medical Device Control Office of the Department of Health has received a report of a serious adverse event associated with intracatheter dilators used with cen Add to Reading List Source URL: www.mdco.gov.hk Language: English - Date: 2013-01-04 02:25:14 Port Peripheral venous catheter Central venous catheter Urinary catheterization Remote magnetic navigation Medicine Catheters Technology
35	CALVARY HEALTH CARE ADELAIDE – HUMAN RESEARCH AND ETHICS COMMITTEE Document number: CHCA – HREC 1.7 Created on: 23 November 2011 Approved by: CHCA HREC Last review: 22 November 2013 Page 1 of 2 Custodian: Nancy Olsze Add to Reading List Source URL: www.calvarynorthadelaide.org.au Language: English - Date: 2014-07-30 03:58:59 Scientific method Science Safety monitoring Adverse event Serious adverse event Institutional review board Clinical research Pharmaceutical industry Research
36	CALVARY HEALTH CARE ADELAIDE – HUMAN RESEARCH AND ETHICS COMMITTEE Document number: CHCA – HREC 1.7 Created on: 23 November 2011 Approved by: CHCA HREC Last review: 22 November 2013 Page 1 of 2 Custodian: Nancy Olsze Add to Reading List Source URL: www.calvarycentraldistricts.org.au Language: English - Date: 2014-07-30 03:58:59 Scientific method Science Safety monitoring Adverse event Serious adverse event Institutional review board Clinical research Pharmaceutical industry Research
37	INVESTIGATOR SERIOUS ADVERSE EVENT (SAE) REPORT Add to Reading List Source URL: www.ranzco.edu Language: English - Date: 2014-06-10 23:41:15 Informed consent Pharmaceutical industry Food and Drug Administration Behavior Clinical research coordinator Medical ethics Clinical research Ethics
38	NUS Institutional Review Board (IRB) REPORT OF SERIOUS ADVERSE EVENTS or UNANTICIPATED EVENTS NUS Institutional Review Board (IRB) Add to Reading List Source URL: www.nus.edu.sg Language: English - Date: 2013-10-14 02:45:17 Pharmacology Pharmaceutical sciences Science Design of experiments Medical ethics Adverse event Institutional review board Serious adverse event Food and Drug Administration Clinical research Pharmaceutical industry Research
39	Quality Account July[removed]June 2013 Enhancing the health and independence of the people of South Canterbury www.scdhb.health.nz Add to Reading List Source URL: www.hqsc.govt.nz Language: English - Date: 2014-07-10 18:35:55 Pharmaceutical industry Medical terms Patient safety Hospice Adverse event Clinical governance District Health Board Serious adverse event Patient safety organization Medicine Health Clinical research
40	EUROPEAN COMMISSION DIRECTORATE GENERAL for HEALTH and CONSUMERS Consumer Affairs Cosmetics and Medical Devices MEDDEV 2.7/3 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-11-27 04:23:55 Technology Research Medical equipment European Union directives Medical device Medical technology Adverse event Serious adverse event Medical Devices Directive Clinical research Medicine Pharmaceutical industry

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