European Medicines Agency and Heads of Medicines Agencies (2012) Guideline on Good Pharmacovigilance Practices (GVP)—Module VI Management and Reporting of Adverse Reactions to Medicinal Products. - References

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European Medicines Agency and Heads of Medicines Agencies (2012) Guideline on Good Pharmacovigilance Practices (GVP)—Module VI: Management and Reporting of Adverse Reactions to Medicinal Products.

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