Certificate of pharmaceutical product - PDFSEARCH.IO - Document Search Engine

Certificate of pharmaceutical product
Results: 101

#	Item
81	Application for extended term of a medicinal product’s SPC Regulation (EU) No[removed] Add to Reading List Source URL: www.prv.se Language: English - Date: 2014-06-27 03:28:08 Patent law Law Pharmaceutical industry Term of patent Marketing authorization Patent application Patent Government Intellectual property law Patent law of the European Union Supplementary protection certificate
82	Application for SPC for plant protection productsRegulation (EU) No[removed] Add to Reading List Source URL: www.prv.se Language: English - Date: 2014-06-27 02:39:56 Marketing authorization Pharmaceuticals policy Summary of Product Characteristics Term of patent Patent Law Government Supplementary protection certificate Intellectual property law Pharmaceutical industry Patent law
83	Microsoft Word - Report 2010.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:12:00 Pharmacology Pharmaceutical industry European Medicines Agency Pharmaceuticals policy Supplementary protection certificate Summary of Product Characteristics Directive 2001/83/EC Food and Drug Administration Clinical research Pharmaceutical sciences Research
84	Microsoft Word - Report 2009.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:11:59 Pharmaceutical sciences Pharmaceuticals policy European Medicines Agency Government Supplementary protection certificate Summary of Product Characteristics Directive 2001/83/EC Clinical research Research Pharmaceutical industry
85	The European Agency for the Evaluation of Medicinal Products Inspections MRA Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-10-18 12:54:01 Marketing authorization Certificate of pharmaceutical product Pharmaceutical industry Pharmaceuticals policy Good manufacturing practice
86	GENERAL OVERVIEW ABOUT THE CURRENT EXTENSION OF TEST DATA PROTECTION IN LATINAMERICA1 The term “Test Data “ or “Registration Data” refers to the information gathered in the pre-clinical and clinical stages carrie Add to Reading List Source URL: www.ipo.org Language: English - Date: 2013-03-31 18:57:45 Pharmacology Health Drug discovery Patent law Marketing authorization Test data exclusivity Certificate of pharmaceutical product Agreement on Trade-Related Aspects of Intellectual Property Rights Orphan drug Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry
87	Report on Paediatric regulations 2011 Corr Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:12:00 European Medicines Agency Pharmaceutical sciences Supplementary protection certificate Pharmacology Summary of Product Characteristics Clinical research Pharmaceutical industry Research
88	Annual report 2013 on benefits and infringements (art 50) Paed regulation - Corr1 June 2014 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-06-20 02:57:41 European Medicines Agency Pharmaceutical sciences Supplementary protection certificate Pharmaceutics Summary of Product Characteristics Clinical research Pharmaceutical industry Research
89	Annual report 2012 on benefits and infringements (art 50) Paed regulation - Correction 2 June 2014 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-06-20 02:57:41 Pharmaceutical sciences European Medicines Agency Pharmaceutics Supplementary protection certificate Summary of Product Characteristics Validation Clinical research Pharmaceutical industry Research
90	Microsoft Word - Chap 2 rev 2007 Feb 14 clean fin.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:50 Clinical research Health Drug safety Pharmacy Summary of Product Characteristics Directive 2001/83/EC Pharmacovigilance Supplementary protection certificate Qualified Person for Pharmacovigilance Pharmaceuticals policy Pharmaceutical sciences Pharmacology