Is your regulatory intelligence actually built for Pharmacovigilance?

Most safety teams are already keeping up with regulatory change. The updates get read, the alerts get forwarded, the spreadsheet gets another row. So why does pharmacovigilance still feel like firefighting?

The honest answer is that general regulatory affairs monitoring was never built for PV. It catches plenty, but it doesn't give you a process you can actually stand behind when someone asks you to prove what you decided and why.

In this conversation, Alexandra Constantinescu, our Head of PV Intelligence, sits down with Dr. Jan Petracek to get into what regulatory intelligence built for PV really takes, including the small everyday habit that quietly leaves teams unable to prove their decisions when it matters most.

If your regulatory intelligence feels more like scrambling than a process, this one is worth your time.

Got a question of your own? Put it to a PV expert at ivigee.com. A real, considered answer, no sales pitch.

By Gemma Dailly

Marketing Director

Gemma Dailly is Marketing Director at iVigee and a seasoned marketing professional with extensive experience across clinical research and healthcare technology. Having held senior marketing roles at CluePoints and AARDEX Group, she specialises in building high-growth brands, developing strategic marketing programmes, and turning complex industry challenges into compelling stories that resonate with customers and stakeholders alike.

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