EudraVigilance

Results: 183



#Item
41Accessing MedDRA ICH developed the Medical Dictionary for Regulatory Activities (MedDRA) to help standardise and streamline communication of medical information between regulators and pharmaceutical companies. MedDRA is

Accessing MedDRA ICH developed the Medical Dictionary for Regulatory Activities (MedDRA) to help standardise and streamline communication of medical information between regulators and pharmaceutical companies. MedDRA is

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Source URL: www.ich.org

Language: English - Date: 2014-12-16 09:39:59
429 April 2013 EMARev 1* Guideline on good pharmacovigilance practices (GVP) Module II – Pharmacovigilance system master file (Rev 1)

9 April 2013 EMARev 1* Guideline on good pharmacovigilance practices (GVP) Module II – Pharmacovigilance system master file (Rev 1)

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Source URL: www.ema.europa.eu

Language: English - Date: 2013-07-21 06:33:00
43EX_Fly-Prod_PcVmanager_2014.indd

EX_Fly-Prod_PcVmanager_2014.indd

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Source URL: www.extedo.com

Language: English - Date: 2014-09-02 09:08:02
44GPG ME_Recording Coding Reporting Assessment I_DRAFT_PC

GPG ME_Recording Coding Reporting Assessment I_DRAFT_PC

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Source URL: static.correofarmaceutico.com

Language: English - Date: 2015-04-14 11:52:45
45Ref. AresEUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA

Ref. AresEUROPEAN 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 09:30:39
46GPG ME_Recording Coding Reporting Assessment I_DRAFT_PC

GPG ME_Recording Coding Reporting Assessment I_DRAFT_PC

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Source URL: www.ema.europa.eu

Language: English - Date: 2015-04-14 08:59:35
47Clinical research / Pharmaceutical sciences / Pharmaceutical industry / Drug safety / Patient safety / Pharmacovigilance / Adverse effect / EudraVigilance / Adverse event / Medicine / Health / Pharmacology

Contents Section 1: Legislation 5

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Source URL: www.medsafe.govt.nz

Language: English - Date: 2015-04-01 21:02:22
48EU Draft Guidance on Medication Errors Consultation with EC’s PSQCWG Patient Safety and Quality of Care Working Group meeting, Brussels 18 December 2014 Presented by: Dr. Thomas Goedecke Best Evidence Development, Euro

EU Draft Guidance on Medication Errors Consultation with EC’s PSQCWG Patient Safety and Quality of Care Working Group meeting, Brussels 18 December 2014 Presented by: Dr. Thomas Goedecke Best Evidence Development, Euro

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Source URL: ec.europa.eu

Language: English - Date: 2015-01-15 05:52:16
49  	
   	
      Position Paper

        Position Paper

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Source URL: www.efpia.eu

Language: English - Date: 2013-10-23 09:49:38
50HAI EUROPE RESPONSE Amsterdam, 2 March 2009 Response to the Public consultation on the draft Eudra Vigilance Access Policy for medicines for human use  This response has been prepared by Health Action International (HAI)

HAI EUROPE RESPONSE Amsterdam, 2 March 2009 Response to the Public consultation on the draft Eudra Vigilance Access Policy for medicines for human use This response has been prepared by Health Action International (HAI)

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Source URL: www.haiweb.org

Language: English - Date: 2010-02-27 01:35:31