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21	Medicinal products for human use Add to Reading List Source URL: www.europarl.europa.eu Language: English - Date: 2015-04-01 15:07:10 Pharmaceutical sciences Health European Medicines Agency EudraLex Pharmacovigilance Clinical Trials Directive Directive 2001/83/EC Medicines and Healthcare products Regulatory Agency Directive 65/65/EEC Clinical research Pharmaceuticals policy Research
22	Information for Applicants / Holders of Marketing Authorisation for Veterinary Medicinal Products with respect to the implementation of the Commission Regulation (EC) No[removed]concerning the examination of variation Add to Reading List Source URL: www.uskvbl.cz Language: English - Date: 2010-02-11 03:34:07 Research Health Pharmaceutical industry EudraLex European Union law Pharmacology Marketing authorization European Medicines Agency Qualified Person Responsible For Pharmacovigilance Pharmaceuticals policy Clinical research Pharmaceutical sciences
23	Qualified Persons in the Pharmaceutical Industry Code of Practice 2009, revised February 2013 Add to Reading List Source URL: www.rsc.org Language: English - Date: 2014-07-15 10:30:27 Pharmaceutical sciences Health Qualified Person EudraLex Good manufacturing practice Validation Directive 2001/83/EC Quality assurance Clinical Trials Directive Pharmaceuticals policy Clinical research Research
24	Notice of the ISCVBM regarding submission of application and dossier Add to Reading List Source URL: www.uskvbl.cz Language: English - Date: 2010-02-11 04:20:41 Digital media Grants EudraLex Electronic submission Validation Science Scientific method Learning Marketing authorization Clinical research Pharmaceuticals policy Pharmaceutical industry
25	Legislative Council Secretariat IN19[removed]INFORMATION NOTE Regulations governing the definition, registration and Add to Reading List Source URL: www.legco.gov.hk Language: English - Date: 2014-07-15 02:23:42 Research Health Pharmaceutical industry Pharmacology European Union European Medicines Agency EudraLex Directive 2001/83/EC Marketing authorization Pharmaceuticals policy Clinical research Pharmaceutical sciences
26	PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO- OPERATION SCHEME 2 February 2015 EMA/INS/GMP[removed] Add to Reading List Source URL: www.picscheme.org Language: English - Date: 2015-02-10 05:55:58 Good manufacturing practice Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme Business EudraLex Quality management system Technology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical industry Pharmaceuticals policy Health
27	Kliiniset elinlketutkimukset Add to Reading List Source URL: www.fimea.fi Language: English - Date: 2011-03-14 06:08:11 Pharmaceutical sciences Pharmacology Pharmaceuticals policy Pharmacy European Medicines Agency EudraLex Clinical trial Good Clinical Practice Veterinary physician Clinical research Research Pharmaceutical industry
28	From: Ondrušová Stela [mailto:[removed]] Sent: Wednesday, March 19, [removed]:45 AM To: SANCO PHARMACEUTICALS D5 Cc: Slaný Jozef; Kovácsová Šárka; [removed] Subject: FW: External st Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-11-13 06:49:42 Pharmaceutical sciences European Union Health Pharmacology European Medicines Agency Directive 2001/83/EC Medicinal product Clinical Trials Directive EudraLex Clinical research Pharmaceuticals policy Research
29	Falsified Medicines The mysteries of the Falsified Medicines Directive – where is the logic on safety features? The European Commission says that pharmaceutical companies whose products are not covered by the Falsifie Add to Reading List Source URL: www.cov.com Language: English - Date: 2015-02-13 10:43:11 Clinical research Pharmacology Drug safety Drugs Over-the-counter drug EudraLex Association of the British Pharmaceutical Industry Medical device Pharmaceutical Management Agency Pharmaceuticals policy Medicine Health
30	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 663 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-10-24 08:50:49 Pharmacology Health Pharmaceutical industry Pharmacy European Medicines Agency Directive 65/65/EEC EudraLex Veterinary Medicines Directorate Pharmaceuticals policy Clinical research Pharmaceutical sciences