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Serious adverse event
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11	REPORTING SERIOUS ADVERSE EVENTS (SAEs) AND PROBLEMS INVOLVING RISKS TO SUBJECTS OR OTHERS IN VA RESEARCH A Serious Adverse Advent (SAE) or a Problem Involving Risks to Subjects or Others occurs in VA research. The SAE o Add to Reading List Source URL: www.va.gov Language: English Adverse event Serious adverse event Clinical research Pharmaceutical industry Research
12	3.2 ADVERSE EVENT (AE) PROCESS & FORMS Serious Adverse Events (SAEs), Suspected Unexpected Serious Adverse Reactions (SUSARs), annual trial safety updates and other related safety information are Add to Reading List Source URL: www.sjog.org.au Language: English - Date: 2014-10-30 00:26:29 Pharmacology Science Health Design of experiments Patient safety Clinical trial Adverse effect Institutional review board Serious adverse event Clinical research Research Pharmaceutical industry
13	PDF Document Add to Reading List Source URL: www.research.ucsf.edu Language: English - Date: 2012-10-24 18:40:41 Pharmaceutical sciences Pharmacology Pharmaceutics Adverse event Serious adverse event Food and Drug Administration Clinical research Pharmaceutical industry Research
14	SERIOUS ADVERSE EVENT REPORT FORM (FORM 3.1) Whenever there is any SAE event in any research approved by the Davao Doctors Hospital Institutional Ethics Review Committee, it has to be reported by the principal investigat Add to Reading List Source URL: www.ddh.com.ph Language: English - Date: 2014-07-27 21:56:29 Data transmission Protocols Informed consent Medical ethics Information Communications protocol
15	PDF Document Add to Reading List Source URL: www.hqsc.govt.nz Language: English - Date: 2014-10-28 16:03:58 Medical terms Clinical research Pharmaceutical industry Healthcare Health care in New Zealand Adverse event District Health Board Serious adverse event Health care provider Medicine Health Patient safety
16	ANNEX 1 AFSerious Adverse Event Report Principal Investigator: …………………………………….. Study Site: Add to Reading List Source URL: www.health.gov.bt Language: English - Date: 2014-11-24 01:41:35 Serious adverse event Adverse event Clinical research Pharmaceutical industry Research
17	PDF Document Add to Reading List Source URL: www.hqsc.govt.nz Language: English - Date: 2014-10-28 16:40:04 Clinical research Pharmaceutical industry Medical terms Patient safety District Health Board Health care in New Zealand Serious adverse event Adverse event Ministry of Health Medicine Health Healthcare in New Zealand
18	MDH_IRB FORM 3(G)2012: SERIOUS ADVERSE EVENT/S REPORTSerious Adverse Event/s Report Principal Investigator: Add to Reading List Source URL: www.maniladoctors.com.ph Language: English - Date: 2014-05-11 23:03:26 Medicine Health Adverse event Adverse effect Serious adverse event DD/MM/YYYY Reaction Science Clinical research Pharmaceutical industry Pharmacology
19	DOC Document Add to Reading List Source URL: www.eyeandear.org.au Language: English - Date: 2015-02-19 22:31:52 Research Health Pharmacology Design of experiments Epidemiology Adverse event Clinical trial Serious adverse event Adverse effect Clinical research Pharmaceutical industry Medicine
20	25 SeptemberEMA/CHMPCommittee for Medicinal Products for Human Use (CHMP) Assessment report Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2014-12-17 05:29:48 Research Drug safety Pharmacology European Medicines Agency Pharmaceuticals policy Committee for Medicinal Products for Human Use International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacovigilance Serious adverse event Clinical research Pharmaceutical sciences Pharmaceutical industry

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