The fundamental driving force of pharmacovigilance is the safeguarding of public health.
Pharmacovigilance is a multi and cross-area discipline that deals with incidence and frequency of adverse events of pharmaceuticals and medical devices worldwide.
The reporting of adverse events is critical to the creation of a valid pharmacovigilance program that can identify adverse events before they have an impact on public health. However, language can be a barrier in the reporting process. In many instances, adverse events and databases are reported in the local language.
In this guide we explore the:
- Role of pharmacovigilance in public health and safety
- Key stakeholders, contributors and tools
- Key strategies to establishing best practices in translations
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