Guideline on good pharmacovigilance practices (GVP) Module VI – Management and reporting of adverse reactions to medicinal pro
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Guidelines on good pharmacovigilance practices (GVP) Introductory cover note, last updated with draft revision 2 of module V on
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Eu2P Short Course: GVP Module VI - Collection, management and submission of reports of suspected ADR to Medicinal Products
Guideline on good pharmacovigilance practices (GVP) - Module VI – Collection, management and submission of reports of suspecte
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