Who we are
Claritas Genomics serves children affected with complex genetic disorders by providing timely and accurate results, resolving families’ long search for answers. By combining clinical expertise of the world’s best pediatric specialists with innovative platform solutions, Claritas is working to improve patient care and enable new discoveries. We are committed to the highest quality and accessibility of information and our interpretive services and unique approach to reporting set the standard for reliably and clearly communicating genetic information. Now is the time to integrate genomics into clinical practice to inform, guide and improve medical treatment for kids around the world.
Claritas offers services that support all aspects of the clinical testing experience, from test ordering to providing the most reliable and up-to-date clinical report for each patient. Our tests are derived from the clinical expertise at pediatric hospitals and, if requested, we can connect our clients to subject matter experts for follow-up.
As part of our mission to partner with health care providers to improve patient care, Claritas Genomics is deeply committed to creating resources that further our community’s knowledge about genetics and genomics. Check back often as our content will continue to grow.
Claritas was created to broaden access to the medical genomics expertise in the pediatric community. The company is majority owned and controlled by pediatric hospitals and is connecting the networked hospitals to promote sharing of infrastructure in genetic testing, data for research, expertise and best practices. For more on membership please contact us.