With 95% of rare diseases lacking an FDA-approved product for treatment, the need for information about rare diseases and the people they impact is greater than ever.
By adding RWD to the equation, researchers and developers can make clinical trials more efficient by finding under-diagnosed patients and creating longitudinal patient journeys, rich with insights across the time continuum.
Join HealthVerity on May 27th to explore ways in which we can help you close the gap in rare disease research and build detailed patient profiles for commercial teams with access to the largest RWD ecosystem.
During this webinar, you’ll uncover how to:
- Access and connect RWD like medical and pharmacy claims, lab tests and results, EMR data (and more) to build detailed patient profiles
- Follow short and long-term clinical outcomes in specific patient cohorts to track disease progression
- Better understand consumer and lifestyle factors that may cause complications or adverse effects in patients