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Serious adverse event
Results: 260

#	Item
201	Canada Vigilance Adverse Reaction Reporting Form Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-06-24 11:44:52 Medical terms Patient safety Adverse effect Health Canada Clinical research Serious adverse event Medicine Health Pharmacology
202	ROF letter A_doc_correctedalt Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Health Interferon Peginterferon alfa-2a Adverse effect MedWatch Serious adverse event Antivirals Medicine Cytokines
203	SAMPLE FORMAT FOR SERIOUS OR UNEXPECTED ADVERSE EVENT REPORT Add to Reading List Source URL: www.usafa.edu Language: English - Date: 2012-11-27 09:57:06 Health Medicine Pharmacology Food and Drug Administration Patient safety Adverse event Serious adverse event Adverse effect Clinical trial Clinical research Pharmaceutical industry Research
204	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE Final Concept Paper E2F: Development Safety Update Report dated 7 September 2006 Endorsed by the ICH S Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:14:08 Health International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical trial Environmental Working Group Serious adverse event Council for International Organizations of Medical Sciences Pharmacovigilance Adverse event Clinical research Research Pharmaceutical sciences
205	Microsoft Word - HeartWare System Redacted Briefing Book, May 7th.doc Add to Reading List Source URL: www.fda.gov Language: English Ventricular assist device Adverse event Investigational Device Exemption Serious adverse event Clinical research Pharmaceutical industry Medicine
206	Microsoft Word - E2F_Example_Commercial_DSUR.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:14:02 Health Medicine Pharmacology Design of experiments Medical terms Clinical trial Adverse effect Adverse event Serious adverse event Clinical research Pharmaceutical industry Research
207	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED TRIPARTITE GUIDELINE Add to Reading List Source URL: private.ich.org Language: English - Date: 2006-03-06 03:47:53 Health Clinical research Pharmaceutical industry Drug safety Pharmacy Pharmacovigilance Adverse effect Adverse event Serious adverse event Pharmacology Pharmaceutical sciences Medicine
208	Microsoft PowerPoint - AE Provision - DRAFT[removed]Compatibility Mode] Add to Reading List Source URL: prsinfo.clinicaltrials.gov Language: English - Date: 2014-03-11 16:44:01 Pharmaceutics Pharmaceutical sciences Clinical trial Adverse event Serious adverse event Clinical research Pharmaceutical industry Research
209	Microsoft PowerPoint - HCPs EN Jan 12_07.pps Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-07-09 12:42:51 Pharmacology Patient safety Adverse effect Sertraline Antidepressant Major depressive disorder Serious adverse event Pharmacovigilance Medicine Health Medical terms
210	FDA’s Adverse Event Surveillance Systems and MedWatch Add to Reading List Source URL: www.fda.gov Language: English Health Medicine Clinical research Pharmaceutical industry MedWatch Pharmacovigilance Clinical trial Adverse Event Reporting System Serious adverse event Pharmacology Pharmaceutical sciences Food and Drug Administration

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