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Qualified Person for Pharmacovigilance
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#	Item
1	B.08 GUIMA Transfer national requirements AT BE CZ DE(BVL, PEI) EE ES FI FR IE IS IT LT LV NL PL RO SE SK SI UKEMA-CMDv Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-02-02 09:57:36 Pharmaceuticals policy Health care Health Pharmaceutical industry Medical research Healthcare quality European Medicines Agency European Union Qualified Person Responsible For Pharmacovigilance Marketing authorization Summary of Product Characteristics Pharmacovigilance
2	CMDv GUIPartial MAH transferEMA-CMDv Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-06-03 11:37:56 Pharmaceuticals policy Health care Health Healthcare quality Pharmaceutical industry Medical research Drug safety Agencies of the European Union Qualified Person for Pharmacovigilance European Medicines Agency Pharmacovigilance Marketing authorization
3	COMMISSION OF THE EUROPEAN COMMUNITIES Brussels, 10 December 2008 SECVolume I Add to Reading List Source URL: www.myereport.eu Language: English - Date: 2015-11-08 06:14:30 Pharmaceuticals policy Health Medical research Pharmacovigilance European Medicines Agency EudraLex European Directive on Traditional Herbal Medicinal Products Postmarketing surveillance Adverse effect Qualified Person Responsible For Pharmacovigilance EudraVigilance
4	Better vigilance for health health protection protection and and innovation Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2015-06-23 05:26:42 Pharmaceuticals policy Medical research Health European Medicines Agency Pharmacovigilance Qualified Person Responsible For Pharmacovigilance EudraVigilance
5	JuneApplication Form for Renewal of a Marketing Authorisation Add to Reading List Source URL: www.nmvrvi.lt Language: English - Date: 2015-01-22 12:42:09 Pharmacology Research Drug safety Pharmacy Health Qualified Person Pharmacovigilance Supplementary protection certificate European Medicines Agency Clinical research Pharmaceuticals policy Pharmaceutical sciences
6	Microsoft Word - Volume IX ENdoc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:59:58 Health Medicine Pharmaceuticals policy Drug safety Pharmacy Pharmacovigilance EudraLex Qualified Person Responsible For Pharmacovigilance Postmarketing surveillance Pharmacology Pharmaceutical sciences Clinical research
7	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
8	Study on the Availability of Medicinal Products for Human Use Specific Request EAHC/2011/Health/14 for the Implementation of Framework Contract EAHC/2010/Health/01 Lot 1 Add to Reading List Source URL: ehtpa.eu Language: English - Date: 2014-12-15 12:15:41 Pharmaceutical sciences Health European Directive on Traditional Herbal Medicinal Products European Medicines Agency Directive 2001/83/EC Supplementary protection certificate Qualified Person Responsible For Pharmacovigilance Clinical research Pharmaceuticals policy Research
9	EN Official Journal of the European Union Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:55:57 European Union Pharmaceutical industry Pharmaceutical sciences Government European Medicines Agency Directive 2001/83/EC Supplementary protection certificate Qualified Person Responsible For Pharmacovigilance Pharmaceuticals policy Clinical research Research
10	INFORMED CONSENT APPLICATIONS IN MUTUAL RECOGNITION AND DECENTRALISED PROCEDURES RECOMMENDATIONS Doc. Ref.: CMDhRev.4 April 2015 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-04-29 06:02:55 Pharmaceutical industry Pharmaceuticals policy Pharmacology Qualified Person for Pharmacovigilance Consent Criminal law Law

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