Technology has a critical role to play in helping patients, and the clinicians and institutions they trust, make every moment matter in the fight against cancer.

This blog represents an ideas exchange on how exciting new innovation could be applied to assist at each step in the patient pathway.

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FDA's Response to the Proposed Exemption of Section 510(k) Requirements

By Richard Morroney, RAC, CQA On April 21, 2021

FDA's Response to the Proposed Exemption of Section 510(k) Requirements

On January 15, 2021, the Department of Health and Human Services (HHS) issued a Notice in the Federal Register that, among...

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Topics: digital pathology, regulation, FDA,

The Community Has Spoken in Favor of Digital Pathology: Survey Results

By Emil Mladenov On March 5, 2021

The Community Has Spoken in Favor of Digital Pathology: Survey Results

A proposal in the January 15 2021 Federal Register took the Pathology community by surprise and created quite the excitement...

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Topics: digital pathology, regulation, FDA,

New FDA Pronouncement Paves the Way for Digital Pathology's Rise

By Richard Morroney, RAC, CQA On January 25, 2021

New FDA Pronouncement Paves the Way for Digital Pathology's Rise

When COVID-19 surprised us in early 2020, digital pathology providers had few FDA-cleared options to leverage their solutions,...

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Topics: digital pathology, regulation, FDA,

All-Time High Support of Digital Pathology Driven by COVID-19

By Dr Martin Stuart On June 23, 2020

All-Time High Support of Digital Pathology Driven by COVID-19

The COVID-19 pandemic has wreaked havoc on healthcare systems across the world as we have struggled to contain the spread of...

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Topics: Post-COVID-19, digital pathology, regulation,

The Over-Regulation of Digital Pathology Systems

By Richard Morroney, RAC, CQA On June 5, 2020

The Over-Regulation of Digital Pathology Systems

Why does it take a pandemic to reset overly burdensome medical device regulations?Whole slide imaging (WSI) system technology...

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Topics: digital pathology, regulation, FDA,