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Directive 2001 83 EC
Results: 312

#	Item
161	Flowchart for Determing the Regulatory Status of Tissue and Cell-Based Products (Version 4) Donated / procured tissue and cells Human or animal ? Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2009-12-15 11:44:07 European Union Law Health Directive 2001/83/EC Clinical Trials Directive Medical device European Directive on Traditional Herbal Medicinal Products Directive 93/41/EEC Pharmaceuticals policy Clinical research Medicine
162	Joint Industry Position Paper on Economic Operators Introduction The medical technology industry welcomes the introduction of provisions regarding economic operators within the European Commission proposed regulations on Add to Reading List Source URL: www.euromcontact.org Language: English - Date: 2014-07-12 08:52:38 Medical equipment Medical technology European Union Pharmaceuticals policy Medical device Medical Devices Directive Directive 2001/83/EC Good Laboratory Practice European Authorized Representative Medicine Technology European Union directives
163	[removed]EN Official Journal of the European Union Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:24:06 Pharmaceutical sciences Health European Medicines Agency Directive 2001/83/EC EudraLex Council Implementing Regulation (EU) No 282/2011 Clinical research Pharmaceuticals policy Research
164	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 614 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:45:39 Health Pharmacology Drug safety Pharmacy Pharmacovigilance Directive 2001/83/EC European Medicines Agency Qualified Person Responsible For Pharmacovigilance Pharmaceuticals policy Pharmaceutical sciences Clinical research
165	Breaches for which the current Infringement Regulation[removed]may be used: Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:36:08 Research Health Pharmacovigilance European Medicines Agency Directive 2001/83/EC Qualified Person Suspected Adverse Reaction Surveillance Scheme Supplementary protection certificate Pharmaceuticals policy Clinical research Pharmaceutical sciences
166	Microsoft Word - Revision_2007_08-FINAL.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:55:14 European Union Pharmacology Pharmaceutical sciences Health Research Summary of Product Characteristics Directive 2001/83/EC European Directive on Traditional Herbal Medicinal Products Supplementary protection certificate Pharmaceuticals policy Clinical research European Union directives
167	Microsoft Word - NBOG_BPG_2009_3.doc Add to Reading List Source URL: www.nbog.eu Language: English - Date: 2014-03-10 03:22:41 Medical equipment Medical device Medical Devices Directive Notified Body IVD Directive 2001/83/EC Medicine Technology Medical technology
168	Review of the Research Exemption (‘Bolar’) Provision as set down in Section 42(g) of the Patents Act[removed]The Department is inviting comments from interested parties on a proposal to broaden the scope of the “Bola Add to Reading List Source URL: www.djei.ie Language: English - Date: 2012-03-06 09:26:09 Law Patent law of the European Union Intellectual property law Patent law Research exemption Government Supplementary protection certificate European Medicines Agency Directive 2001/83/EC Clinical research Pharmaceuticals policy Research
169	IMPORTANT LEGAL NOTICE - The information on this site is subject to a disclaimer and a copyright notice Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:48 Research Health policy Directive 75/319/EEC Directive 65/65/EEC Directive 2001/83/EC Factortame litigation Supplementary protection certificate European Directive on Traditional Herbal Medicinal Products Pharmaceuticals policy Clinical research Law
170	EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL Consumer goods Pharmaceuticals PHARM 529 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:23:50 Medicine Health European Medicines Agency Directive 2001/83/EC Pharmacovigilance Medical device International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical Trials Directive Clinical research Pharmaceuticals policy Research

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