Aim: Identify solutions to the most important policy barriers to the clinical adoption of next-generation sequencing.
Materials & Methods: Four-round modified policy Delphi with a multistakeholder panel of 48 experts. The panel deliberated policy solutions to (previously reported) challenges deemed most important to address.
Results: The group advocated using consensus panels to promote consistency in payer policies and to standardize test reporting, and favored making genomic data-sharing a condition of regulatory clearance, certification, or accreditation processes. They were split on the role of US FDA.
Conclusion: Panelists found common ground on solutions for health plan coverage policy consistency, data-sharing, and standardizing reporting, but were sharply divided on the role of the FDA in mitigating risks to patients.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722256 | PMC |
http://dx.doi.org/10.2217/pme-2016-0104 | DOI Listing |
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