COVID-19 has changed clinical trial monitoring now and in the future. The problem is that sites are limited by fragmented technology that makes it difficult to remotely access study information across email, phone, video, and other systems.
How can sites share information and engage with monitors in a compliant way, while ensuring quality and efficiency in the future? Watch this webinar to see how Veeva is putting sites, sponsors, and CROs in a stronger position to respond to this crisis and improve clinical trials in the long term.
Speakers: