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European Medicines Agency
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21	The Agency for Medicinal Products and Medical Devices of the Republic of Slovenia has prepared the unofficial consolidated text for the Medicinal Products Act which includes:  Medicinal Products Act (Official Gazette Add to Reading List Source URL: www.jazmp.si Language: English - Date: 2013-07-12 06:13:47 Pharmaceuticals policy Health Medical research Clinical Trials Directive Directive 2001/83/EC Good laboratory practice Marketing authorization Good Clinical Practice Directive European Pharmacopoeia Biopharmaceutical Pharmacovigilance European Medicines Agency
22	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
23	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
24	HTGH CMDh GUIDANCE DOCUMENTS Published on CMDh Website (http://www.hma.eu/cmdh.html) Documents Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-05-17 04:19:48 Medical research Agencies of the European Union Business Economy European Medicines Agency European Union Pharmaceutical industry Administrative guidance Validation
25	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
26	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
27	TIGes Vet - Terms of Reference-June 2012 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:08 Agencies of the European Union European Medicines Agency European Union Veterinary physician Health Government
28	Q & A for EMA eSubmission Gateway Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:47 Medical research Health Clinical data management Clinical research Electronic common technical document Pharmaceutical industry Agencies of the European Union European Medicines Agency Form Marketing authorization Email
29	eSubmission Gateway / Web Client to become mandatory for all eCTD submissions through the centralised Procedure in 2014 <> "Error"eSubmission Gateway / Web Client to become mandatory for all eCTD submissions through th Add to Reading List Source URL: esubmission.ema.europa.eu Language: English* - Date: 2016-08-19 03:14:51 Medical research Clinical data management Clinical research Health Electronic common technical document Digital media Research Common Technical Document European Medicines Agency Electronic submission Form EMA
30	01 June 2015 EMAInformation Technology Electronic Application Form Data Exchange Standard 3.0 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:30 RDM Stage lighting Marketing authorization Maa European Medicines Agency Health Government