Communicate scientific information effectively, improve regulatory compliance and manage safety operations efficiently
Existing medical operations are
Suboptimal
to meet changing expectations on medical and scientific content
Unscalable
to meet growing volume of adverse events being reported
Overstretched
to comply with rapidly changing regulations across markets
73%
medical affairs operations are unable to personalize medical information
16.9 million
adverse events were reported to the US FDA from 2013-22
90%
of regulatory operations’ technology maturity is basic
What we do
Adopt technology to accelerate and scale medical outcomes
Personalize physician, patient and payer experience
We enable medical affairs organizations with core domain expertise and technology to deliver consistent and customized medical and scientific information
Reduce total cost of pharmacovigilance operations
We empower safety teams with insights and technology to proactively monitor, analyze and report adverse event signals and manage risks effectively
Improve success and speed of regulatory approvals
Our life sciences-contextualized technology across the product development lifecycle ensures 100% compliance in a complex and dynamically changing regulatory landscape