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Adverse event
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391	University of Central Oklahoma Add to Reading List Source URL: www.uco.edu Language: English - Date: 2014-09-12 09:25:53 Ethics Science Pharmacology Drug safety Design of experiments Institutional review board Adverse event Serious adverse event Risk Clinical research Research Pharmaceutical industry
392	Vaccine Safety: Parent Handout Add to Reading List Source URL: www2.aap.org Language: English - Date: 2009-12-07 13:05:29 Vaccination Drug safety Public safety Vaccine Adverse Event Reporting System Vaccine injury Vaccine Influenza vaccine Varicella vaccine Medicine Vaccines Prevention
393	Appendix Abbreviations AEFI adverse event following immunisation AIDS acquired immunodeficiency syndrome Add to Reading List Source URL: www.health.gov.au Language: English - Date: 2013-09-04 01:15:49 Vaccination Pediatrics Mumps Measles MMRV vaccine MMR vaccine Varicella vaccine Pertussis Pneumococcal conjugate vaccine Medicine Health Vaccines
394	Sydney University Human Research Ethics Committee Notification Form: Adverse incidents (non-clinical trial research) This form should be used to report ALL adverse incidents in non-clinical trial research. Add to Reading List Source URL: sydney.edu.au Language: English - Date: 2014-09-10 02:20:16 Design of experiments Pharmaceutical industry Pharmacology Applied ethics Medical ethics Clinical trial Research ethics Institutional review board Adverse event Clinical research Research Science
395	6ème Journée et Prix de la Recherche Clinique Présentations orales _________________________________________________________________________________ NIFURTIMOX-EFLORNITHINE COMBINATION THERAPY (NECT) FOR SECOND-STAGE Add to Reading List Source URL: www.hug-ge.ch Language: English - Date: 2015-01-06 11:28:02 Antiprotozoal agents Nifurtimox African trypanosomiasis Eflornithine Pharmacovigilance Trypanosomiasis Adverse event Médecins Sans Frontières Medicine Chemistry Organic chemistry
396	Sydney University Human Research Ethics Committee REPORTING Form: Adverse events In clinical trials THIS FORM SHOULD BE USED TO REPORT: Adverse Events (AEs), Serious Adverse Events (SAEs), Serious Unexpected Suspected Dr Add to Reading List Source URL: sydney.edu.au Language: English - Date: 2014-10-03 02:00:37 Pharmaceutics Pharmaceutical sciences Adverse event Clinical trial Serious adverse event Communications protocol Research ethics Clinical research Pharmaceutical industry Research
397	Sydney University Human Research Ethics Committee REPORTING Form: SUMMARY REPORT FORM OF ADVERSE EVENTS FOR CLINICAL TRIALS THIS FORM SHOULD BE USED TO REPORT: For Annual Serious Adverse Events (SAEs) And Quarterly/Six M Add to Reading List Source URL: sydney.edu.au Language: English - Date: 2014-10-03 02:00:37 Pharmacology Health Pharmaceutical sciences Adverse effect Serious adverse event Adverse event Irma Clinical trial Clinical research Pharmaceutical industry Research
398	Microsoft Word - GCP Course_Agenda_ENG_web.docx Add to Reading List Source URL: www.wwctrials.com Language: English - Date: 2013-01-04 12:08:16 Science Pharmaceutics Clinical trial Adverse event Clinical research Pharmaceutical industry Research
399	Microsoft Word - Copy of Summary of Pharmacovigilance Systems _SPS_ Guidance notes version 15 Apr-2013.doc Add to Reading List Source URL: www.gov.uk Language: English - Date: 2013-12-18 07:52:24 Pharmaceutical sciences Pharmacovigilance Adverse effect Black triangle Medical device Adverse event Qualified Person Responsible For Pharmacovigilance Qualified Person for Pharmacovigilance Pharmacology Medicine Health
400	TERMS OF REFERENCE DATA & SAFETY MONITORING BOARD Effectiveness of a simplified short regimen for Multidrug Resistant Tuberculosis treatment in Karakalpakstan, Uzbekistan Add to Reading List Source URL: fieldresearch.msf.org Language: English - Date: 2014-10-14 22:57:21 Médecins Sans Frontières Safety monitoring Adverse event Technology Science Business Clinical research Pharmaceutical industry Data monitoring committees

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