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EudraPharm
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#	Item
11	Update of COMP activities Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 07:36:22 Pharmacology Pharmaceuticals policy Drug safety Clinical research EudraPharm Pharmacovigilance FluMist Summary of Product Characteristics Vaccine Health Pharmaceutical sciences Medicine
12	Microsoft Word - Stakeholders Information_May2009_rev_3.doc Add to Reading List Source URL: www.hma.eu Language: English - Date: 2009-06-24 10:10:02 Pharmaceutical sciences Medicine Clinical research Pharmacology Pharmacovigilance EudraPharm EudraVigilance Pharmaceuticals policy Drug safety Health
13	Microsoft Word - 68_HMA_Stakeholder information_final.docx Add to Reading List Source URL: www.hma.eu Language: English - Date: 2012-02-28 09:40:01 Health Drug safety Research Pharmaceutical industry Pharmacology Pharmacovigilance EudraVigilance EudraPharm Good Clinical Practice Clinical research Pharmaceuticals policy Pharmaceutical sciences
14	Title of Your Presentation Add to Reading List Source URL: www.efanet.org Language: English - Date: 2014-02-21 10:11:55 Research European Medicines Agency Pharmaceutics Alternative medicine Pharmacology EudraPharm Pharmaceutical industry Clinical research Pharmaceutical sciences
15	PDF Document Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:47 Research Health Pharmacology Pharmacy European Union European Medicines Agency Pharmacovigilance Clinical Trials Directive EudraPharm Pharmaceuticals policy Clinical research Pharmaceutical sciences
16	Microsoft Word - Stakeholders Information_May2009_rev_3.doc Add to Reading List Source URL: www.hma.eu Language: English - Date: 2012-02-09 06:17:14 Pharmaceutical sciences Medicine Clinical research Pharmacology Pharmacovigilance EudraPharm EudraVigilance Pharmaceuticals policy Drug safety Health
17	Permettre l’examen simplifié des modifications Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:35:13 Clinical research Health Pharmacy Drug safety European Medicines Agency Pharmacovigilance EudraPharm Directive 2001/83/EC Pharmaceutical industry Pharmaceutical sciences Pharmaceuticals policy Pharmacology
18	Implementing technical guidance – List of fields for result-related information to be submitted to the ‘EudraCT’ clinical tria Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:49 Health Clinical Data Management EudraCT Clinical trials National Institutes of Health ClinicalTrials.gov EudraPharm Clinical trials registry Database Clinical research Research Pharmaceutical industry
19	IP[removed]Brussels, 22nd March 2011 Pharmaceuticals: today, the EU Register of Clinical Trials is launched Online From today, all EU citizens will have access to information on the thousands Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:21 Pharmaceutical sciences Health Pharmaceuticals policy Pharmacology European Medicines Agency Clinical trial Clinical Trials Directive Good Clinical Practice EudraPharm Clinical research Pharmaceutical industry Research
20	Association Européenne des Spécialités Pharmaceutiques Grand Public Association of the European Self-Medication Industry Europäischer Verband der Arzneimittel-Hersteller AESGP comments on the implementing technical g Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:48 Health Clinical Data Management EudraCT Clinical trials Pharmaceuticals policy EudraPharm ClinicalTrials.gov Clinical research Research Pharmaceutical industry