41![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 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](https://www.pdfsearch.io/img/5cdb67e068bdd8c32d99e8d4727e68e3.jpg) | Add to Reading ListSource URL: www.ich.orgLanguage: English - Date: 2014-12-16 09:39:59
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42![9 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)](https://www.pdfsearch.io/img/26c7ddc33f1160f7406951fa7ab3e1c8.jpg) | Add to Reading ListSource URL: www.ema.europa.euLanguage: English - Date: 2013-07-21 06:33:00
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43![EX_Fly-Prod_PcVmanager_2014.indd EX_Fly-Prod_PcVmanager_2014.indd](https://www.pdfsearch.io/img/26de958ca42f0ade675ac5f4fef4db06.jpg) | Add to Reading ListSource URL: www.extedo.comLanguage: English - Date: 2014-09-02 09:08:02
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44![GPG ME_Recording Coding Reporting Assessment I_DRAFT_PC GPG ME_Recording Coding Reporting Assessment I_DRAFT_PC](https://www.pdfsearch.io/img/91385c57e09543f8904ac9d5cd4d3dbf.jpg) | Add to Reading ListSource URL: static.correofarmaceutico.comLanguage: English - Date: 2015-04-14 11:52:45
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45![Ref. 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](https://www.pdfsearch.io/img/20f16dcc15a0152b9eaf2e978b696122.jpg) | Add to Reading ListSource URL: ec.europa.euLanguage: English - Date: 2013-10-09 09:30:39
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46![GPG ME_Recording Coding Reporting Assessment I_DRAFT_PC GPG ME_Recording Coding Reporting Assessment I_DRAFT_PC](https://www.pdfsearch.io/img/c6cdc285953d82e0df2956f572ad8cd0.jpg) | Add to Reading ListSource URL: www.ema.europa.euLanguage: English - Date: 2015-04-14 08:59:35
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47![Clinical research / Pharmaceutical sciences / Pharmaceutical industry / Drug safety / Patient safety / Pharmacovigilance / Adverse effect / EudraVigilance / Adverse event / Medicine / Health / Pharmacology Clinical research / Pharmaceutical sciences / Pharmaceutical industry / Drug safety / Patient safety / Pharmacovigilance / Adverse effect / EudraVigilance / Adverse event / Medicine / Health / Pharmacology](/pdf-icon.png) | Add to Reading ListSource URL: www.medsafe.govt.nzLanguage: English - Date: 2015-04-01 21:02:22
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48![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 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](https://www.pdfsearch.io/img/df8fedb08e365d899a5212e12a92eef8.jpg) | Add to Reading ListSource URL: ec.europa.euLanguage: English - Date: 2015-01-15 05:52:16
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49![Position Paper
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50![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) 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)](https://www.pdfsearch.io/img/51ee1b7401f2996a6f8fa25abc00af60.jpg) | Add to Reading ListSource URL: www.haiweb.orgLanguage: English - Date: 2010-02-27 01:35:31
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