Streamline pharmacovigilance delivery to meet safety demands

You have increasing opportunities to validate your drug’s safety. But, the proliferation of new data sources, resource pressures and expanding regulatory requirements is making pharmacovigilance challenging and difficult to scale.

That’s why our expert safety teams are harnessing the power of innovative smart machines and automation to design, build and execute streamlined end-to-end safety solutions, while reducing costs.

IQVIA’s ability as a single vendor to provide safety services across your product’s lifecycle is unmatched.

See how our global experience and innovative approach can help you manage your pharmacovigilance needs from clinical through post marketing.

Harness IQVIA's Full Power

Introducing the IQVIA CORE™, the new way we'll innovate.

Pharmacovigilance Automation and Digital Governance
Simplify your adverse events process by completely replacing internal monitoring and tracking activities.