Qualified Person for Pharmacovigilance

Results: 136



#Item
111EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA  PHARM 617

EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 617

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 08:48:55
112UKPAR CEFUROXIME 250MG POWDER FOR SOLUTION FOR INJECTION AND CEFUROXIME 1.5G POWDER FOR SOLUTION FOR INJECTION OR INFUSION PL[removed]Cefuroxime 250mg powder for solution for injection

UKPAR CEFUROXIME 250MG POWDER FOR SOLUTION FOR INJECTION AND CEFUROXIME 1.5G POWDER FOR SOLUTION FOR INJECTION OR INFUSION PL[removed]Cefuroxime 250mg powder for solution for injection

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Source URL: www.mhra.gov.uk

Language: English - Date: 2014-06-18 05:51:10
113Public Consultation Paper Review of Commission Regulation (EC) n° [removed]Final EFPIA/EVM/EBE comments) General comments Company

Public Consultation Paper Review of Commission Regulation (EC) n° [removed]Final EFPIA/EVM/EBE comments) General comments Company

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:34:54
114CMDh QUESTIONS & ANSWERS RENEWALS Doc. Ref.: CMDh[removed], Rev0 November[removed]APPLICATION FOR THE RENEWAL OF A MARKETING

CMDh QUESTIONS & ANSWERS RENEWALS Doc. Ref.: CMDh[removed], Rev0 November[removed]APPLICATION FOR THE RENEWAL OF A MARKETING

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Source URL: www.hma.eu

Language: English - Date: 2012-11-22 06:13:01
115Marketing authorization / Validation / Qualified Person for Pharmacovigilance / Drug Master File / Pharmaceutical industry / Pharmaceutical sciences / Pharmacology

DOC Document

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Source URL: www.hma.eu

Language: English - Date: 2014-06-13 11:13:48
116Microsoft Word - final  minutes 13th vetpharm com.doc

Microsoft Word - final minutes 13th vetpharm com.doc

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:22:02
117EUROPEAN COMMISSION Brussels, [removed]SWD[removed]final

EUROPEAN COMMISSION Brussels, [removed]SWD[removed]final

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:40:09
118Ref. Ares[removed][removed]EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products — authorisations, EMA

Ref. Ares[removed][removed]EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products — authorisations, EMA

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:28:03
119Commission Implementing Regulation (EU) No[removed]of 7 March 2013 on the selection of a symbol for the purpose of identifying medicinal products for human use that are subject to additional monitoringText with EEA rele

Commission Implementing Regulation (EU) No[removed]of 7 March 2013 on the selection of a symbol for the purpose of identifying medicinal products for human use that are subject to additional monitoringText with EEA rele

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 08:55:12
120EUROPEAN COMMISSION ENTERPRISE DIRECTORATE-GENERAL Single market, regulatory environment, industries under vertical legislation Pharmaceuticals and cosmetics  VETPHARM 187

EUROPEAN COMMISSION ENTERPRISE DIRECTORATE-GENERAL Single market, regulatory environment, industries under vertical legislation Pharmaceuticals and cosmetics VETPHARM 187

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Source URL: ec.europa.eu

Language: English - Date: 2013-10-09 09:25:08