You might know that it is challenging to monitor and track Adverse Drug Reactions and Adverse Events as a part of Pharmacovigilance activities. To address the challenges, from June 30, 2022, the Pharmacovigilance Risk Assessment Committee (PRAC) mandated ICSR reporting in the ISO format in the EU. Decode how this can enhance the reporting process. Watch this short video. [ Ссылка ] #Pharmacovigilance #AdverseDrugReactions #AdverseEvents #ICSRReporting #ISOFormat #Automation #EMA #HMA #ShortClip #FreyrSolutions

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