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1	1 AugustElectronic Application Forms are now fully available for use For initial marketing authorisation (human and veterinary), variation and renewal applications Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:40 Pharmaceuticals policy Health Medical research Clinical data management Clinical research Pharmaceutical industry European Union EudraLex European Medicines Agency Electronic common technical document Common Technical Document Marketing authorization
2	eAF Question and Answers - update-KM_CPh-KP Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:02 Medical research Health Clinical data management Clinical research Pharmaceuticals policy European Medicines Agency European Union EudraLex Electronic common technical document Validation
3	emea_strap_url_cmyk_rev_en_std_cent.eps MASTER Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-07-08 04:50:21 Pharmaceuticals policy Health Pharmaceutical industry Pharmacology European Medicines Agency European Union Marketing authorization European Directorate for the Quality of Medicines EudraLex European Pharmacopoeia Orphan drug Supplementary protection certificate
4	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
5	CMDh IP meeting November 2015 eSubmission Karin Gröndahl Head of Registration and Information Management, MPA, Sweden Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-11-27 10:35:36 Medical research Clinical data management Clinical research Health Electronic common technical document Pharmaceutical industry Digital media Electronic submission EudraLex Validation
6	EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL Consumer goods Pharmaceuticals Brussels, Add to Reading List Source URL: sfbct.free.fr Language: English - Date: 2013-09-12 15:12:41 Medical research Pharmaceuticals policy Clinical research Pharmaceutical industry European Union directives European Union Clinical Trials Directive Good Clinical Practice Directive Clinical trial EudraLex Good clinical practice Traceability
7	Transfer of information contained in Notice to Applicants, Volume 6A, Chapter 7 (Nov 2012) Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-06-15 05:38:46 Pharmaceuticals policy Marketing authorization Health EudraLex Gui Personal life
8	Microsoft Word - Volume IX ENdoc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:59:58 Health Medicine Pharmaceuticals policy Drug safety Pharmacy Pharmacovigilance EudraLex Qualified Person Responsible For Pharmacovigilance Postmarketing surveillance Pharmacology Pharmaceutical sciences Clinical research
9	Correspondence an atmosphere that is still chilly towards primary care. There has been further growth in specialisation, with diﬀerences in income and status Add to Reading List Source URL: ethikkommission.meduniwien.ac.at Language: English - Date: 2010-04-27 10:49:02 Medicine Clinical Trials Directive Good Clinical Practice EudraLex Clinical trials registry General practitioner Clinical trial Clinical research Research Health
10	Current Global GMP Status and Trends With Focus on EU & PIC/S JPMA Annual Meeting, Tokyo & Osaka, September 2012 Dr.-Ing. Stephan Rönninger Pharma Medicines Technical Operations Global Quality & Compliance, F. Hoffmann- Add to Reading List Source URL: www.jpma.or.jp Language: English - Date: 2013-06-30 20:57:12 Quality Pharmaceutical sciences Research Business Validation Qualified Person Good distribution practice EudraLex Medicinal product Pharmaceuticals policy Clinical research Pharmaceutical industry

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