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61	ROADMAP TITLE OF THE INITIATIVE TYPE OF INITIATIVE Revision of Veterinary Pharmaceutical Legislation CWP Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-12-20 07:57:04 Pharmaceutical sciences Health European Medicines Agency Pharmaceutical industry Veterinary Medicines Directorate EudraLex Clinical research Pharmaceuticals policy Research
62	VETERINARY MEDICINES DIRECTORATE AND VETERINARY PRODUCTS COMMITTEE OPEN MEETINGS[removed]am, Wednesday 8 October 2014 Add to Reading List Source URL: www.vmd.defra.gov.uk Language: English - Date: 2014-10-13 04:31:54 Medicine Pharmaceutical industry European Medicines Agency Executive agencies of the United Kingdom government Veterinary Medicines Directorate Pharmacovigilance EudraLex Summary of Product Characteristics Veterinary physician Pharmaceutical sciences Clinical research Pharmacology
63	19 April 2013 EMA[removed]Rev 1* Guideline on good pharmacovigilance practices (GVP) Module VIII – Post-authorisation safety studies (Rev 1) Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2013-07-21 06:33:01 Health Pharmaceuticals policy Pharmaceutical industry Drug safety Pharmacovigilance European Medicines Agency Clinical trial Pharmacoepidemiology EudraLex Pharmaceutical sciences Pharmacology Clinical research
64	INTERNATIONAL CONGRESS AND 53 rd ANNUAL MEETING OF THE SOCIETY FOR MEDICINAL PLANT RESEARCH (GA) AND THE SOCIETÀ ITALIANA DI FITOCHIMICA (SIF[removed]2005, FLORENCE, ITALY Add to Reading List Source URL: www.ga-online.org Language: English - Date: 2008-12-31 12:37:02 Clinical research Pharmaceuticals policy Drug safety European Directive on Traditional Herbal Medicinal Products European Union Pharmacology Pharmacovigilance European Medicines Agency EudraLex Pharmaceutical sciences Health Medicine
65	21 May 2014 EMA[removed]Compliance and Inspections Department Guidance for the template for the qualified person’s declaration concerning GMP compliance of active Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2014-06-16 07:12:26 Research Pharmaceutical sciences Health Qualified Person Good manufacturing practice European Medicines Agency EudraLex Validation Medicinal product Clinical research Pharmaceuticals policy Pharmaceutical industry
66	AD HOC WORKING GROUP ON VALIDATION ISSUES/NATIONAL REQUIREMENTS POSITION PAPER COMMON GROUNDS SEEN FOR INVALIDATION/ DELAYING DAY 0 Doc. Ref.: CMDh[removed]Rev0Rev1 September 2008December 2010 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2011-01-05 07:37:04 Validity Quality Validation EudraLex Science Business Technology Clinical research Pharmaceutical industry Pharmaceuticals policy
67	Guidelines for phase 1 clinical trials 2012 edition Foreword The development of new and better medicines is vital for the public health. A key step in Add to Reading List Source URL: www.sehta.co.uk Language: English - Date: 2012-08-20 09:05:15 Pharmaceutical industry Health Pharmaceuticals policy Pharmacology Drug discovery Clinical trial Pharmacovigilance EudraLex Clinical Trials Directive Clinical research Research Pharmaceutical sciences
68	PDF Document Add to Reading List Source URL: www.efgcp.be Language: English - Date: 2010-03-03 05:45:48 Good Clinical Practice Clinical trial Clinical Trials Directive Ethics Committee Pharmacovigilance EudraLex European Organisation for Research and Treatment of Cancer Academic clinical trials EudraCT Clinical research Research Pharmaceutical sciences
69	PDF Document Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:08 Pharmaceutical sciences Ethics Committee Clinical Trials Directive EudraLex Medical research Clinical trial Clinical pharmacology European Association for Clinical Pharmacology and Therapeutics Clinical research Research Health
70	PDF Document Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2009-02-09 06:26:17 Research Pharmacology Pharmacy Pharmaceutical industry European Medicines Agency Supplementary protection certificate Pharmacovigilance EudraLex Clinical Trials Directive Pharmaceutical sciences Clinical research Pharmaceuticals policy