Consistent and standardized reporting practices for clinical genomic tests are essential for efficient laboratory operations. Without universal adoption, current processes will continue to inhibit:
– Cross-platform interoperability
– Data mining, reuse, and aggregation
– Payer and audit readiness
– Downstream genomic clinical decision support (gCDS) tools

We're heading to the Festival of Genomics and Biodata in Boston June 24-25 at the Boston Convention & Exhibition Center to sit down with clinical reference laboratories and talk about how Leap Consulting Group can help them streamline workflows, standardize reporting, implement modern LIMS, and even consolidate their clinical, revenue cycle, research, and patient access systems.

If that sounds like something your lab could benefit from, contact us to set up a meeting in Boston with our Managing Partner, Josh Kramer, or our Practice Principal, Life Sciences, Heather E. Williams, PHD, MBA, MS, PGD, ERCLG, CG(ASCP)MB. Let's talk!

You can find out more about the Festival of Genomics and Biodata and register here.

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