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Guideline on good pharmacovigilance practices (GVP) · medicinal product and an occurrence is suspected. 154 For regulatory reporting purposes, as detailed in the ICH-E2D guideline,
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ICH - EFPIA · 2018-04-10 · E2A Clinical Safety Data Management: DefiniJon and Standard of Report E2D Post-Approval Safety Data Management E2B Clinical Safety Data Mgm: Data Factors
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ICH - E2D Pharmacovigilance and Drug Safety - Professor Peivand Pirouzi
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