A New York Minute: US FDA Leverages State's Health Department To Expedite NGS Reviews
The agency authorized a next-generation sequencing tumor profiling system that leverages the New York State Department of Health to speed future clearances.
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FDA Looks To Whittle Down Dx Review Load With Pre-Certs, Third-Party Assists
US FDA Commissioner Scott Gottlieb and the agency’s new diagnostics office chief Tim Stenzel want to use a combination of pre-certification, assistance from third-party reviewers and review exemptions to help quickly clear the tsunami of molecular-based diagnostic tests expected to be submitted to FDA for review in the next several years.
FDA Pathway Options Are Growing For Diagnostics, FDA's Gottlieb Tells Commercial Labs
While lab-developed test (LDTs) remain under a US FDA enforcement discretion policy, the agency is working on several fronts to offer appealing regulatory pathways for advanced diagnostic services, FDA Commissioner Scott Gottlieb told American Clinical Laboratory Association members.
Diagnostics 2018: Steady Progress And The Big Get Bigger
If the beginning of 2017 was marked by doubts around whether and how the FDA would act with respect to complex diagnostics, we enter 2018 feeling that slow-moving vessel may finally be turning.