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Pharmacovigilance
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21	PDF Document Add to Reading List Source URL: www.efpia.eu Language: English - Date: 2016-04-04 06:14:49 Medical research Health Clinical trials Clinical research Pharmaceuticals policy Drug discovery Pharmaceutical industry Pharmacovigilance European Federation of Pharmaceutical Industries and Associations ClinicalTrials.gov European Medicines Agency Clinical Trials Directive
22	COMMISSION OF THE EUROPEAN COMMUNITIES Brussels, 10 December 2008 SECVolume I Add to Reading List Source URL: www.myereport.eu Language: English - Date: 2015-11-08 06:14:30 Pharmaceuticals policy Health Medical research Pharmacovigilance European Medicines Agency EudraLex European Directive on Traditional Herbal Medicinal Products Postmarketing surveillance Adverse effect Qualified Person Responsible For Pharmacovigilance EudraVigilance
23	ZAI Lab announces appointment of Dr. James Yan as Executive Vice President of Early Development and Drug Safety Shanghai, China – October – Zai Lab Limited (Zai Lab), an innovative biotech company based in Ch Add to Reading List Source URL: www.zailaboratory.com Language: English - Date: 2015-10-23 03:31:24 Medical research Health Clinical research Drug safety Pharmaceutical industry Drug discovery Food and Drug Administration Pharmacovigilance Drug development Hospira Phases of clinical research Covance
24	EU Module 1 eCTD Specification VersionMay 2016 Document Control Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:42 Medical research Clinical research Computing Clinical data management Health Electronic common technical document Pharmaceuticals policy Markup languages Common Technical Document Marketing authorization Pharmacovigilance Document type definition
25	FACULTY OF HEALTH AND MEDICAL SCIENCES UNIVERSITY OF COPENHAGEN Copenhagen Centre for Regulatory Science (CORS) Medical Product Innovation - Research & Education Add to Reading List Source URL: pharmacy.ku.dk Language: English - Date: 2015-11-20 05:42:08 Medical research Science and technology Health care Clinical research Biopeople Biotechnology Regulatory science Pharmacy Regulatory affairs Pharmacovigilance
26	Agenda Scottish Health Informatics Programme (SHIP) Annual Retreat Add to Reading List Source URL: www.scot-ship.ac.uk Language: English - Date: 2014-04-01 08:13:47 Medical research Health care Health Pharmaceuticals policy Clinical research Clinical trials Drug safety Healthcare quality Pharmacovigilance Health informatics
27	Pharmacovigilance certificate Add to Reading List Source URL: www.chiralindia.com Language: English - Date: 2016-08-13 13:39:00 Chemistry Nature Stereochemistry Enantioselective synthesis Chirality RS Chiral column chromatography Fine chemical
28	Document Type Doc ID Status Add to Reading List Source URL: www.astrazeneca.com Language: English - Date: 2016-07-12 10:02:17 Medical research Clinical research Research Clinical trial Good clinical practice Declaration of Helsinki Health informatics Pharmacovigilance Bioethics Human subject research Electronic health record AstraZeneca
29	WWW.CIOMS.CH June 2016 \| Newsletter # 15 Add to Reading List Source URL: www.cioms.ch Language: English - Date: 2016-07-05 04:11:32 Medical research Health Clinical research Pharmaceuticals policy Pharmaceutical industry World Health Organization Drug safety Council for International Organizations of Medical Sciences Pharmacovigilance MedDRA International Federation of Pharmaceutical Manufacturers & Associations Food and Drug Administration
30	EU Module 1 eCTD Specification Version 3.0 October 2015 Document Control Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:42 Medical research Clinical research Clinical data management Health Computing Pharmaceuticals policy Electronic common technical document Markup languages Common Technical Document Marketing authorization Pharmacovigilance Document type definition