Fighting the FDA’s Final Rule on LDTs
CEO Laurie Menser discusses the Association for Molecular Pathology’s court case against the FDA’s rule on laboratory-developed tests.
CEO Laurie Menser discusses the Association for Molecular Pathology’s court case against the FDA’s rule on laboratory-developed tests.
How the MolDX® program works, what it covers, and how it can support better test access, use, and reimbursement in the clinical lab
In an era when genetic and genomic testing are theoretically affordable and accessible, why do so many patients remain undiagnosed?
The current landscape of molecular hematopathology—and what steps clinical labs can take to stay at the forefront of the discipline
Labs that invested heavily in POC molecular tests during COVID-19 are well positioned to leverage this equipment toward GAS diagnostics