Over 80% of rare diseases may be genetic in origin, and have a significant impact on our healthcare system. Children with rare disease often have a long diagnostic journey, taking over 7 years to reach a diagnosis through 8 different physicians and nearly $20,000 invested in the wrong genetic tests.
Join us and experience the value of clinical genome sequencing. You will understand what genome sequencing is and is not, how it changed the life of one family, and how clinicians use it. Learn how access and use a value assessment tool to see if genome sequencing can benefit your population.
Click here for additional information and registration details.
Related Content
Evidence Matters 2022
Evidence Matters is a virtual one-day summit that brings the literature review community together from different industries to learn, engage, and solve ever-pressing evidence-based research challenges.
Accelerating the Generation of Payer Insights and Evidence Across the Product Lifecycle to Achieve Optimal Access
Experts will present opportunities for using agile platforms and fit-for-purpose engagement models that can drive an iterative approach to obtaining payer insights and developing impactful evidence generation strategies.
Making HEOR More Accessible to Patients
Join this panel discussion to hear experts from patient advocacy, health literacy, and Health Economics and Outcomes Research (HEOR).