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News Daily News

‘Hey, ChatGPT: Surgery or the Cath Lab?’ Study Shows AI Can Aid Decision-Making

Yael L. Maxwell

August 14, 2024

News Daily News

Two New Studies Highlight Lack of Diversity in Cardiovascular RCTs

Michael O'Riordan

July 11, 2023

News Daily News

STEMI Mortality Unaffected by Weekend, Weeknight, or Holiday Admission in France

Michael O'Riordan

October 31, 2019

News Daily News

High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

Michael O'Riordan

July 20, 2018

News Daily News

FDA Takes on 3-D Printing in Healthcare With Initial Guidance Document

Yael L. Maxwell

December 06, 2017

News Daily News

Medical Devices Approved More Quickly in EU Face More Safety Alerts and Recalls

Shelley Wood

July 05, 2016

News Daily News

欧盟更快速核准医疗器械导致更多的安全警告和产品召回

Shelley Wood

July 05, 2016

News Daily News

Los Dispositivos Médicos Aprobados Más Rápidamente en la UE son Objeto de Más Alertas de Seguridad y Nuevas Inspecciones

Shelley Wood

July 05, 2016

News Daily News

New European Device Regulations Are Coming, Could Impact Speed of Approvals

Todd Neale

May 27, 2016

News Daily News

FDA Proposal Seeks to Shine Early Spotlight on Postmarket Device Safety Concerns

Caitlin E. Cox

January 03, 2016

News Conference News TCT 2015

FDA Speaker Outlines a Novel Vision for Device Regulation

October 13, 2015

News Daily News

Leaders from NIH, FDA, Academia Urge US Government to Invest in Medical Innovation

L.A. McKeown

May 09, 2014

News Conference News TCT 2013

Regulatory Hurdles Pose Challenges for Device Approvals in US, Europe

October 30, 2013

News Conference News TCT 2013

TCT Leadership Outlines the State of Intervention

October 30, 2013

News Daily News

NEJM Articles Argue to Sack FDA’s Device Clearance Process

Caitlin E. Cox

August 12, 2011

News Daily News

Commentary Authors Urge Improvements to Device Approval Process

Caitlin E. Cox

July 20, 2011

News Daily News

Report on Device Recalls Criticizes Current FDA Approval Process

L.A. McKeown

February 14, 2011

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‘Hey, ChatGPT: Surgery or the Cath Lab?’ Study Shows AI Can Aid Decision-Making

Two New Studies Highlight Lack of Diversity in Cardiovascular RCTs

STEMI Mortality Unaffected by Weekend, Weeknight, or Holiday Admission in France

High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

FDA Takes on 3-D Printing in Healthcare With Initial Guidance Document

Medical Devices Approved More Quickly in EU Face More Safety Alerts and Recalls

欧盟更快速核准医疗器械导致更多的安全警告和产品召回

Los Dispositivos Médicos Aprobados Más Rápidamente en la UE son Objeto de Más Alertas de Seguridad y Nuevas Inspecciones

New European Device Regulations Are Coming, Could Impact Speed of Approvals

FDA Proposal Seeks to Shine Early Spotlight on Postmarket Device Safety Concerns

FDA Speaker Outlines a Novel Vision for Device Regulation

Leaders from NIH, FDA, Academia Urge US Government to Invest in Medical Innovation

Regulatory Hurdles Pose Challenges for Device Approvals in US, Europe

TCT Leadership Outlines the State of Intervention

NEJM Articles Argue to Sack FDA’s Device Clearance Process

Commentary Authors Urge Improvements to Device Approval Process

Report on Device Recalls Criticizes Current FDA Approval Process

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