Collaboration between sponsors, CROs and sites is an ongoing challenge in clinical trials, especially with document exchange and management.
Sites are overwhelmed by the many sponsor portals used for document exchange, continuing to spend considerable time organizing their paper ISFs.
Sponsors, on the other hand, remain concerned about quality, tracking, and inspection readiness. These combined challenges consume time that sites could be focusing on study participants, recruitment and overall study management.
Join this webinar to learn the steps Veeva has taken to address these challenges by enabling seamless process execution and data flow across patients, sites, and sponsors/CROs to create a connected clinical ecosystem.
Key learning objectives:
- How to improve collaboration between sponsors, CROs and sites
- Create a connected clinical ecosystem
- Enable seamless process execution and data flow
Speakers:
Adam Kohegyi
Senior Consultant, Vault Clinical Operations / EU Digital Trials Lead
Marie-Claire Flavin
Director, Customer Success
