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Qualified Person for Pharmacovigilance
Results: 136

#	Item
61	EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL Add to Reading List Source URL: www.lakemedelsverket.se Language: English - Date: 2009-03-19 06:42:41 Pharmacology Health Clinical research Drug safety Supplementary protection certificate European Medicines Agency Qualified Person for Pharmacovigilance Drug Master File Marketing authorization Pharmaceutical sciences Pharmaceuticals policy Pharmaceutical industry
62	Microsoft Word - Veterinary Chapter 1 Marketing Authorisation - rev[removed]final rev.3.1.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:01:08 Health Clinical research Drug safety Pharmacy European Medicines Agency Pharmacovigilance Summary of Product Characteristics Supplementary protection certificate Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Pharmacology Pharmaceuticals policy
63	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-05-08 11:10:45 Research Health Pharmacology European Union Pharmaceutical industry European Medicines Agency Supplementary protection certificate Qualified Person Responsible For Pharmacovigilance Clinical Trials Directive Pharmaceuticals policy Clinical research Pharmaceutical sciences
64	Doc. Ref: CMDh[removed]Rev0 December 2012 Template for letter of Access for an application under Article 10c of Directive[removed]EC (‘informed consent’ application) Add to Reading List Source URL: www.hma.eu Language: English - Date: 2012-12-19 06:35:36 Qualified Person for Pharmacovigilance Drug safety Pharmacology Pharmacy
65	Q&A - Practical transitional measures - PhV Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2013-07-21 06:31:45 Health Pharmaceuticals policy Pharmacy Clinical research Qualified Person for Pharmacovigilance Pharmacovigilance European Medicines Agency EudraVigilance Pharmaceutical drug Pharmaceutical sciences Pharmacology Drug safety
66	Medicinal Products Act, No[removed] Add to Reading List Source URL: eng.velferdarraduneyti.is Language: English - Date: 2014-02-07 09:18:48 Pharmacology Health Drug safety Pharmacy Qualified Person Responsible For Pharmacovigilance European Medicines Agency Summary of Product Characteristics Qualified Person Pharmacovigilance Pharmaceutical sciences Pharmaceuticals policy Clinical research
67	6.1 PHARMACOVIGILANCE PART OF THE CMDh MINUTES[removed]September 2012 meeting Chairperson: Peter Bachmann 1. Add to Reading List Source URL: www.hma.eu Language: English - Date: 2012-10-25 10:25:40 Pharmacy Health Pharmacovigilance Pharmaceuticals policy Agenda Qualified Person Responsible For Pharmacovigilance Pharmacology Pharmaceutical sciences Drug safety
68	REGULATION concerning Marketing Authorisations for Natural Medicinal Products and Registration of Traditional Herbal Medicinal Products, No[removed]. Add to Reading List Source URL: eng.velferdarraduneyti.is Language: English - Date: 2013-06-12 06:10:44 Health Pharmaceutical sciences European Directive on Traditional Herbal Medicinal Products European Medicines Agency Directive 2001/83/EC Herbalism Summary of Product Characteristics Alternative medicine Qualified Person Responsible For Pharmacovigilance Pharmaceuticals policy Clinical research Medicine
69	DOC Document Add to Reading List Source URL: europa.eu Language: English Pharmaceutical sciences Drug safety Pharmaceuticals policy Clinical research Pharmacy Pharmacovigilance Adverse effect Patient safety Qualified Person Responsible For Pharmacovigilance Medicine Health Pharmacology
70	PDF Document Add to Reading List Source URL: europa.eu Language: English Pharmaceutical sciences Pharmaceuticals policy Drug safety Pharmacy Clinical research Pharmacovigilance Patient safety Adverse effect Qualified Person for Pharmacovigilance Medicine Health Pharmacology