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Supplementary protection certificate
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1	Trial results: Modalities and timing of posting VersionAprilInterventional Clinical Trials that ended on or after 21 Julyi.e. the date of finalisation of the programming according to Commission Gui Add to Reading List Source URL: www.clinicaltrialsregister.eu Language: English - Date: 2016-07-13 04:51:15 Medical research Clinical research Health Multi-speed Europe Clinical data management EudraCT Clinical pharmacology European Economic Area Clinical Trials Directive Clinical trial Supplementary protection certificate
2	emea_strap_url_cmyk_rev_en_std_cent.eps MASTER Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-07-08 04:50:21 Pharmaceuticals policy Health Pharmaceutical industry Pharmacology European Medicines Agency European Union Marketing authorization European Directorate for the Quality of Medicines EudraLex European Pharmacopoeia Orphan drug Supplementary protection certificate
3	Question Q202 National Group: Sweden Suède Schweden Title: Add to Reading List Source URL: www.aippi.se Language: English - Date: 2011-10-03 07:50:13 Law Government Foreign relations Patent law United States patent law Compulsory license Patent application Patent European Patent Convention Unitary patent Supplementary protection certificate Term of patent in the United States
4	B.12 AF user guide consolidated vet version EMA Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-07-03 09:05:53 Pharmaceuticals policy Pharmaceutical industry Council of Europe European Directorate for the Quality of Medicines Marketing authorization Bioequivalence Test data exclusivity European Medicines Agency Supplementary protection certificate
5	DOC Document Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2016-07-20 07:22:57 Clinical research Pharmaceutical industry Clinical data management Drug safety Electronic common technical document Supplementary protection certificate European Medicines Agency Summary of Product Characteristics Pharmacovigilance Validation Drug Master File
6	CMDh QUESTIONS & ANSWERS GENERIC APPLICATIONS Doc. Ref.: CMDh, Rev.1 AprilSUBMISSION OF A DESCRIPTION OF PHARMACOVIGILANCE SYSTEM AND EU RISK Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-05-16 05:10:10 Pharmaceuticals policy Pharmaceutical industry Clinical research Drug safety Healthcare quality Bioequivalence Summary of Product Characteristics Marketing authorization Test data exclusivity Pharmacovigilance Supplementary protection certificate European Medicines Agency
7	e-News No.40 February 2015 Add to Reading List Source URL: aippi.org Language: English - Date: 2015-08-26 18:39:42 Intellectual property law Trademark Copyright law of the United States Copyright Intellectual property Limitations and exceptions to copyright Supplementary protection certificate
8	Application for grant of a Supplementary Protection Certificate for a Medicinal Product Danish Patent and Trademark Office Add to Reading List Source URL: iprights.dkpto.org Language: English - Date: 2016-05-17 05:21:58 Law Foreign relations Government Pharmaceutical industry Intellectual property law Marketing authorization Pharmaceuticals policy Supplementary protection certificate European Patent Organisation Patent European Patent Convention Summary of Product Characteristics
9	PIPELINE WATCH Valsartan SPC expires in top EU markets n mid-November, Novartis’ Diovan (valsartan) – “the top-selling branded antihypertensive medication worldwide” – lost supplementary protection certificate Add to Reading List Source URL: www.genericsweb.com Language: English - Date: 2011-11-23 17:12:17
10	Application for paediatric extension of a Supplementary Protection Certificate for a Medicinal Product Please consult the Guide for filling in the Application for paediatric extension of a Supplementary Protection Certif Add to Reading List Source URL: iprights.dkpto.org Language: English - Date: 2016-05-17 05:23:18 Foreign relations Law Government Intellectual property law Patent law of the European Union Supplementary protection certificate Patent law Pharmaceutical industry Marketing authorization European Patent Convention Term of patent Patent application