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Directive 65 65 EEC
Results: 32

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1	Better protecting the patients Be aware of the system Add to Reading List Source URL: www.pharmacovigilance2012.nl Language: English - Date: 2011-11-29 08:04:15 Drug safety Pharmaceutical sciences Pharmacology Pharmacy Pharmacovigilance Rofecoxib Elixir sulfanilamide Directive 65/65/EEC Sulfonamide Medicine Health Pharmaceuticals policy
2	JUDGMENT OF THE COURT 9 April 2015 (Veterinary medicinal products – Supplementary protection certificate – Regulation (EEC) No – Concept of “first authorisation to place a product on the market” in t Add to Reading List Source URL: www.eftacourt.int Language: English - Date: 2015-04-09 05:16:30 Intellectual property law Patent law of the European Union Supplementary protection certificate Pharmaceutical sciences Government European Medicines Agency Directive 65/65/EEC Term of patent Qualified Person Responsible For Pharmacovigilance Clinical research Pharmaceuticals policy Research
3	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
4	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
5	BEST PRACTICE GUIDE FOR THE EXCHANGE OF REGULATORY AND ADMINISTRATIVE INFORMATION REGARDING ORPHAN MEDICINAL PRODUCTS BETWEEN THE EMEAEMA AND THE NATIONAL COMPETENT AUTHORITIES October 2003 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2011-11-25 05:34:30 Pharmacology Test data exclusivity Orphan drug Directive 65/65/EEC Directive 75/319/EEC European Medicines Agency Supplementary protection certificate Pharmaceuticals policy Health Pharmaceutical sciences
6	BEST PRACTICE GUIDE FOR THE EXCHANGE OF REGULATORY AND ADMINISTRATIVE INFORMATION REGARDING ORPHAN MEDICINAL PRODUCTS BETWEEN THE EMA AND THE NATIONAL COMPETENT AUTHORITIES Doc. Ref.: CMDh[removed], Rev2 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2011-11-25 05:34:29 Pharmaceutical sciences Pharmacology Orphan drug Test data exclusivity Directive 65/65/EEC Directive 75/319/EEC European Medicines Agency Supplementary protection certificate Pharmaceuticals policy Clinical research Health
7	Risk regulation at international, European and national level The Registration and Authorisation of Homeopathic Medicinal Products in the EU and The Netherlands Author: Johan Hulshof Add to Reading List Source URL: www.riskregulation.org Language: English - Date: 2008-01-18 08:02:01 Medicine Health Directive 2001/83/EC European Directive on Traditional Herbal Medicinal Products Directive 65/65/EEC Regulation and prevalence of homeopathy Directive 93/41/EEC Pharmaceuticals policy Clinical research Research
8	Risk regulation at international, European and national level MARKETING OF MEDICINAL PRODUCTS IN EUROPE: THE ABRIDGED PROCEDURE FOR MARKETING AUTHORISATION AUTHOR: Janske van Santvoort Add to Reading List Source URL: www.riskregulation.org Language: English - Date: 2008-01-17 11:13:05 Health policy Health Directive 2001/83/EC Directive 75/318/EEC Directive 75/319/EEC Directive 65/65/EEC Directive 93/41/EEC Supplementary protection certificate Pharmaceuticals policy Clinical research Research
9	COMMISSION REGULATION (EC) No …/… of […] laying down the provisions for implementation of the criteria for designation of a medicinal product as an orphan medicinal product and definitions of the concepts “simila Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-11-12 03:09:45 Pharmacology Research Health Medicinal product Medical device Directive 65/65/EEC Biologic Alternative medicine European Medicines Agency Clinical research Pharmaceuticals policy Medicine
10	AESGP WELCOMES NEW CPMP OFFICERS AND MEMBERS Add to Reading List Source URL: www.aesgp.eu Language: English Research Pharmacology Pharmaceutical industry Drug safety Executive agencies of the United Kingdom government Pharmacovigilance Medicines and Healthcare products Regulatory Agency Directive 65/65/EEC European Medicines Agency Clinical research Pharmaceutical sciences Pharmaceuticals policy

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