Advanced real world evidence studies for regulatory and reimbursement use
A turnkey solution for regulatory-grade real world evidence studies
Verantos
Collaboratively design study protocol Contract for EHR data Perform de-identification Deploy NLP and AI Implement study protocol Support independent data validation Prepare for publication or regulatory support
Pharma
Collaboratively design study protocol Review each study stage
Academic medical center
Perform IRB review Securely share data Review independent data validation Publish as appropriate