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European Medicines Agency
Results: 2389

#	Item
11	BPGAutomatic validationEMA-CMDv Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-07-27 07:09:22 Pharmaceutical industry Medical research Health care Pharmacology Validity Clinical data management Clinical research Quality Validation Marketing authorization European Medicines Agency
12	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
13	Microsoft Word - E-submission Roadmap Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:14:40 Agencies of the European Union European Union European Medicines Agency Digital media Research Heads of Medicines Agencies Health Electronic submission Government Veterinary physician
14	28 September 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 03:15:35 RDM Stage lighting Marketing authorization European Medicines Agency Health Government
15	B.08 GUIMA Transfer national requirements AT BE CZ DE(BVL, PEI) EE ES FI FR IE IS IT LT LV NL PL RO SE SK SI UKEMA-CMDv Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-02-02 09:57:36 Pharmaceuticals policy Health care Health Pharmaceutical industry Medical research Healthcare quality European Medicines Agency European Union Qualified Person Responsible For Pharmacovigilance Marketing authorization Summary of Product Characteristics Pharmacovigilance
16	Error! No text of specified style in document. <> "Error"eSubmission Gateway Web Client \ MERGEFORMAT eSubmission Gateway Web Client Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:14:59 Health Agencies of the European Union Clinical data management Clinical research Electronic common technical document Digital media European Medicines Agency Knowledge Filename Computing Form Electronic submission
17	Centre européen de biologie et de génomique structurales (CEBGS), unité 964 "Institut de génétique et de biologie moléculaire et cellulaire (IGBMC), Illkirch. Add to Reading List Source URL: www.irdirc.org Language: English - Date: 2016-08-03 05:20:55 Medical research Health Drug discovery Clinical research Epidemiology Pharmaceuticals policy Design of experiments Orphan drug Clinical trial Rare disease European Medicines Agency Draft:Rare Cancers
18	CMDv GUIPartial MAH transferEMA-CMDv Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-06-03 11:37:56 Pharmaceuticals policy Health care Health Healthcare quality Pharmaceutical industry Medical research Drug safety Agencies of the European Union Qualified Person for Pharmacovigilance European Medicines Agency Pharmacovigilance Marketing authorization
19	EMEA/CMDvCMDv/GUI/014 GUIDANCE for The Processing of Generic Applications Through MRP / DCP Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-11-16 09:50:36 Pharmaceutical industry Medical research Pharmacology Clinical research Pharmaceutical sciences Pharmaceuticals policy Marketing authorization Validation Bioequivalence European Medicines Agency
20	Reflection Paper on ethical and GCP aspects of clinical trials Add to Reading List Source URL: www.fercap-sidcer.org Language: English - Date: 2012-05-16 01:59:10 Medical research Health Clinical research Pharmaceutical industry Agencies of the European Union Drug discovery Pharmaceuticals policy European Medicines Agency Heads of Medicines Agencies Clinical trial Good clinical practice Clinical Trials Directive