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European Medicines Agency
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#	Item
31	Better vigilance for health health protection protection and and innovation Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2015-06-23 05:26:42 Pharmaceuticals policy Medical research Health European Medicines Agency Pharmacovigilance Qualified Person Responsible For Pharmacovigilance EudraVigilance
32	Press Release Mylan & Biocon Announce Regulatory Submission for Proposed Biosimilar Pegfilgrastim Accepted for Review by European Medicines Agency BENGALURU, India and HERTFORDSHIRE, England/PITTSBURGH, USA, July 21, 20 Add to Reading List Source URL: www.biocon.com Language: English - Date: 2016-07-21 09:25:25 Biotechnology Biology Medicine Recombinant proteins Specialty drugs Biosimilar Drugs Biopharmaceutical Trastuzumab Mylan Pegfilgrastim Filgrastim
33	Submissions to the PSUR Repository using EMA Gateway/Web Client Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:01 Computing Health Clinical data management Clinical research Data Electronic common technical document Markup languages Computer file formats European Medicines Agency
34	< Company Reference > To: Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-06-15 05:38:43 Agencies of the European Union Pharmaceutical industry European Medicines Agency European Union Marketing authorization Health Government
35	Pharmacovigilance: Information systems and services Supporting business activities of the revised pharmacovigilance Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2015-06-23 05:24:30 Health Pharmaceuticals policy Medical research Drug safety Clinical research Clinical trials Healthcare quality Pharmacovigilance EudraVigilance European Medicines Agency Adverse effect VigiBase
36	23 JanuaryPSUR Repository: Frequently Asked Questions (FAQ) 30 Churchill Place ● Canary Wharf ● London E14 5EU ● United Kingdom +6000 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:04 Open access Academic publishing Agencies of the European Union Knowledge Communication Institutional repository Research European Medicines Agency Academia
37	Microsoft Word - Implementation Plan - QRD template_3 Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2016-02-22 05:36:15 Health Business Pharmacology Pharmaceuticals policy European Medicines Agency European Union Committee for Medicinal Products for Human Use Closure Prescription drug Packaging and labeling
38	Code of Practice for the Promotion of Animal Medicines Together with the Rules of Procedure for the Add to Reading List Source URL: www.noah.co.uk Language: English - Date: 2016-04-25 10:46:34 Health Pharmaceutical sciences Pharmacy in the United Kingdom Executive agencies of the United Kingdom government Veterinary Medicines Directorate Clinical pharmacology Pharmaceuticals policy European Medicines Agency National Office of Animal Health Good laboratory practice Summary of Product Characteristics Paraveterinary workers
39	Microsoft Word - Item 3 i81_HMA Draft Press Release.docx Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-09-17 07:10:39 Agencies of the European Union Heads of Medicines Agencies European Union European Medicines Agency Government Health
40	Technical User Guide eAF hum-vet version20151001-clean Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:01 Medical research Health Pharmaceuticals policy Clinical research Pharmaceutical industry European Union Pharmacopoeias European Medicines Agency European Pharmacopoeia Marketing authorization Electronic common technical document Adobe LiveCycle