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Adverse event
Results: 2359

#	Item
441	Microsoft PowerPoint[removed]Coding_with_MedDRA.pptx Add to Reading List Source URL: www.meddra.org Language: English - Date: 2014-09-23 11:53:36 Health MedDRA EudraVigilance Pharmacovigilance Adverse effect Mental disorder Serious adverse event Pharmaceutical industry Pharmacology Pharmaceutical sciences Medicine
442	CTCAE version 3 Vocabulary Standards Review “Review of the Review” Presented by Salvatore Mungal Add to Reading List Source URL: www.meddra.org Language: English - Date: 2013-03-29 11:03:51 Knowledge representation Technical communication Library science Information science Lexicography Grade Thesaurus Adverse event Advanced Encryption Standard Education Knowledge Science
443	Doc. No. TFDA/DMC/CTPV/003 TANZANIA FOOD AND RUGS AUTHORITY REPORT ON MONITORING OF ADVERSE DRUG REACTIONS DUE TO ANTIMALARIAL Add to Reading List Source URL: www.egov.go.tz Language: English - Date: 2014-11-12 07:17:07 Medicine Pharmacovigilance Uppsala Monitoring Centre Adverse effect Adverse drug reaction Adverse event Artemether Yellow Card Scheme Postmarketing surveillance Pharmacology Pharmaceutical sciences Health
444	Andrea Sloan CURE Act Section-by-Section SECTION 1. SHOT TITLE. The Andrea Sloan Compassionate Use Reform and Enhancement Act, or the Andrea Sloan CURE Act. SEC. 2. EXPANDED ACCESS POLICY AS CONDITION OF EXPEDITED APPROV Add to Reading List Source URL: mccaul.house.gov Language: English - Date: 2014-12-08 13:54:59 Research Clinical research Clinical pharmacology United States Public Health Service Expanded access Investigational New Drug FDA Fast Track Development Program Pharmaceutical industry Adverse event Pharmacology Pharmaceutical sciences Food and Drug Administration
445	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-11-25 13:17:39 Technology Premarket approval Medical device Center for Devices and Radiological Health Breast implant Unique Device Identification Federal Food Drug and Cosmetic Act Breast augmentation Adverse event Medicine Food and Drug Administration Health
446	NIAMS DSM Report Open_Multi-site Open_2014-10-2.docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-24 15:38:08 Case report form Adverse event Safety monitoring Clinical research Pharmaceutical industry Data monitoring committees
447	Federation of the European Academies of Medicine Palais des Académies Rue Ducale 1 B[removed]Brussels Tel: +[removed] Fax: +[removed]65 [removed] www.feam.eu.com FEAM Response to Consultation on Fun Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:50 Science Ethics Committee Clinical trial Clinical Trials Directive Institutional review board EudraCT Serious adverse event Declaration of Helsinki Clinical trial management Clinical research Research Scientific method
448	Comments on the Public Consultation Document Assessment of the functioning of the ‘Clinical Trials Directive’ [removed]EC The Clinical Trial Service Unit ( CTSU) is part of Oxford University and is an academic unit co Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:25 Science Medicine Pharmacology Design of experiments Medical ethics Clinical trial Good Clinical Practice Pharmacovigilance Serious adverse event Clinical research Research Pharmaceutical industry
449	London, 01 February 2010 Doc. Ref. EMA[removed]EUDRAVIGILANCE EXPERT WORKING GROUP COMMENTS ON THE EUROPEAN COMMISSION PUBLIC CONSULTATION PAPER – “ASSESSMENT OF THE FUNCTIONING OF THE “CLINICAL TRIALS Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:49 Pharmaceutical sciences EudraVigilance Serious adverse event Clinical Trials Directive Pharmacovigilance European Medicines Agency Adverse event Clinical trial EudraCT Clinical research Research Health
450	All trials registered. All results reported. September 2013 The AllTrials campaign calls for all past and present clinical trials to be registered and their results reported. Clinical trials are investigations designed t Add to Reading List Source URL: www.alltrials.net Language: English - Date: 2014-05-26 10:34:05 Science Scientific method Clinical trials Design of experiments Epidemiology ClinicalTrials.gov Adverse event Serious adverse event Randomized controlled trial Clinical research Research Pharmaceutical industry

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