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Certificate of pharmaceutical product
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1	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
2	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
3	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
4	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
5	Pursuant to paragraph 4 of Article 94 of the Medicinal Products Act (Official Gazette of the Republic of Slovenia, Nosand 45/08), the Minister of Health, in agreement with the Minister of Agriculture, Forestry an Add to Reading List Source URL: www.jazmp.si Language: English - Date: 2012-06-28 07:16:26 Pharmacology Pharmaceutical sciences Pharmaceutical industry European Medicines Agency Pharmaceuticals policy Summary of Product Characteristics Homeopathy Maintenance fee Supplementary protection certificate Medicine Clinical research Health
6	Name of medicinal product: Procedure number: Module 1: PL=RMS Add to Reading List Source URL: en.urpl.gov.pl Language: English - Date: 2014-05-22 07:32:50 Pharmacology Health Notary Drug safety Qualified Person Responsible For Pharmacovigilance Marketing authorization Pharmacovigilance Public key certificate Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry
7	28 April 2015 EMAHuman Medicines Research and Development Support Division Report to the European Commission on companies and products that have benefited from any of the rewards and Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2015-05-29 07:46:13 Pharmacology Pharmaceutical industry European Medicines Agency Supplementary protection certificate Pharmacovigilance Summary of Product Characteristics EudraCT Clinical research Pharmaceutical sciences Research
8	Application for SPC for plant protection productsRegulation (EU) No Add to Reading List Source URL: www.prv.se Language: English - Date: 2014-10-27 10:26:35 Marketing authorization Pharmaceuticals policy Summary of Product Characteristics Term of patent Patent Law Government Supplementary protection certificate Intellectual property law Pharmaceutical industry Patent law
9	draft revised variation form_clean _EMA-CMD_June 2013 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:55:17 Intellectual property law Patent law of the European Union Supplementary protection certificate Summary of Product Characteristics Test data exclusivity Pharmaceutical drug Pharmaceutical industry Research Clinical research Pharmacology Pharmaceuticals policy Pharmaceutical sciences
10	ΔΔΥΕΠ-Ε.Model statement of licensing status of pharmaceutical product (s) Add to Reading List Source URL: www.eof.gr Language: English - Date: 2012-05-18 05:10:34 Pharmaceuticals policy Pharmaceutical industry Certificate of pharmaceutical product