Insife Webinar Series

Adverse events and other relevant safety information can come from a multiplicity of sources, across clinical research, markets e.g. through programs, literature, spontaneous reporting.

Common for all sources is the presence of source data that needs to be processed and evaluated.

HALOPV will integrate with your current safety database to capture ICSRs and manage follow-ups, and improve the processing of adverse event data between local and global activities. 

Join this webinar to see how HALOPV can increase efficiency across ICSRS and follow-up activities. 

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