Garvit Bindal with over 11 years of experience leading global safety system implementations, migrations, upgrades, and regulatory compliance projects, is a trusted advisor to top pharmaceutical companies on Argus Safety, Veeva Vault Safety, and custom PV solutions. Garvit has managed large-scale case and data migrations exceeding 1 million cases and multi-million documents and has ensured compliance with global PV regulations including EMA, FDA, MHRA, PMDA, MFDS, NMPA, and TFDA. He is recognized for driving strategy, innovation, and operational excellence across pharma and CRO clients worldwide.
For a decade, pharmacovigilance has automated with rules and RPA-fast, but brittle the moment a case or regulation strays from the script. Agentic AI marks a real shift: systems that read, reason, and act across the entire safety lifecycle, from intake and triage to narratives, follow-up, and submission. But not every task wants an agent. This session maps where autonomous AI genuinely adds value, where deterministic scoring and optimization still win, and how the two combine into one governed architecture. Above all, it confronts the question every safety leader is asking: how do you deploy AI across a regulated function-and keep every decision defensible on inspection?