Advamed

Women’s Health Has Come A Long Way. But There’s Still A Long Way To Go

Women’s Health Has Come A Long Way. But There’s Still A Long Way To Go

 

During the Medtech Conference in Toronto, a panel of industry leaders discussed the gaps that remain in women’s healthcare and said innovation can help narrow them.

Passing The Torch: Tarver Addresses Audience At FDA Town Hall, Recognizes Shuren’s Accomplishments

Passing The Torch: Tarver Addresses Audience At FDA Town Hall, Recognizes Shuren’s Accomplishments

 

In her inaugural address to the medtech industry during the Medtech Conference, acting US CDRH director Michelle Tarver described her mission-driven approach.

Lawsuits To Stop FDA From Overseeing LDTs Could Create Chaos, Panelist Says

Lawsuits To Stop FDA From Overseeing LDTs Could Create Chaos, Panelist Says

 

As the 6 May deadline to implement the FDA’s final rule on lab-developed tests approaches, attempts to stop the rule from taking effect are set to play out in court. A panel of experts discussed the potential impact of these legal efforts, should they be successful, at the Medtech Conference in Toronto.

Medtech’s Biggest Leaders Discuss How Innovation Is Shaping The Future Of Health Care

Medtech’s Biggest Leaders Discuss How Innovation Is Shaping The Future Of Health Care

 

During the Medtech Conference in Toronto, three of the industry’s leading CEOs shared their insights into the rapidly changing landscape of health care and how the latest advancements have the potential to make life better for patients everywhere.


Future PCCP Training Coming In Finalized Documents, FDA DHCoE Deputy Director Says

Future PCCP Training Coming In Finalized Documents, FDA DHCoE Deputy Director Says

 
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The AI/ML pre-determined change control plan final guidance will include plans for agency-wide training for the implementation of PCCPs, an FDA deputy director said at the Medtech Conference.

CDRH On Track To Meet All MDUFA V Goals

CDRH On Track To Meet All MDUFA V Goals

 
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CDRH is on track to meet its MDUFA V goals, seeing a steady return to pre-pandemic levels of device authorizations and submissions.

Rulemaking Can Only Do So Much: Stakeholders Weigh In On LDT Rule

Rulemaking Can Only Do So Much: Stakeholders Weigh In On LDT Rule

 
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Investors and business executives weighed in on the FDA’s proposed rule on LDTs during a panel at the Medtech Conference on 9 October. 

Diagnostics Have Evolved, So Too Has the VALID Act, Says FDA’s Hillebrenner

Diagnostics Have Evolved, So Too Has the VALID Act, Says FDA’s Hillebrenner

 

As diagnostics have become more technologically advanced and are used more frequently in detecting diseases, uniform regulatory standards have become necessary, according to a panel of experts discussing testing reform at the MedTech Conference in Boston.