Fig. 1From: A missing link in the bench-to-bedside paradigm: engaging regulatory stakeholders in clinical genomics research a Overview of the regulatory stakeholder relationship established between the Clinical Genome Resource (ClinGen) and the United States Food and Drug Administration (FDA). The two groups defined their common goals and developed transparent communications to seek insight and share progress. b Summary of the dynamics and benefits of partnering with community and regulatory stakeholdersBack to article page