DRAP
The new article provides further clarifications regarding the reporting requirements to be followed in order to ensure that critical information is communicated without undue delay.
DRAP
The new article provides a detailed description of processes and procedures associated with signal management.
DRAP
The new article describes in detail the approach to be followed when it comes to the assessment of adverse events.
DRAP
The new article describes the basics of international collaboration, aimed at further improvement of the regulatory framework and establishing a more efficient information exchange in order to ensure the proper performance of healthcare products as well as the safety of patients.
DRAP
The final article of the cycle provides additional details regarding specific indicators used in the context of a pharmacovigilance system.
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