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News Daily News

Little Pre- and Postmarket Testing for Most Recalled CV Devices

Michael O'Riordan

September 16, 2024

News Conference News SCAI 2024

Women, Black Patients Less Likely to Get Advanced PE Therapy, Analysis Shows

L.A. McKeown

May 06, 2024

News Daily News

Women and Minorities Underrepresented in Heart Valve Trials

L.A. McKeown

July 27, 2023

News Daily News

The More Tweaks Made to PMA-Approved Devices, the More Likely a Recall

Caitlin E. Cox

April 13, 2023

News Daily News

RECORD4 Trial of Rivaroxaban, Published in 2009, Still Turning Heads

Todd Neale

January 19, 2023

News Daily News

More Endpoints, More Problems: FDA Offers Advice for Multi-endpoint Trials

Michael O'Riordan

October 28, 2022

News Daily News

Most Patient-Reported Outcome Measures in CVD Fall Short

L.A. McKeown

September 23, 2022

News Daily News

Postmarketing Studies of CV Devices Still Lacking in the US

Caitlin E. Cox

March 17, 2022

News Daily News

Penumbra’s JET 7 Recall: A Kick Start to Change?

Caitlin E. Cox

December 01, 2021

News Daily News

VASCADE Closure Device: FDA Database Tracks Common Complications, Deaths

Caitlin E. Cox

September 10, 2021

News Daily News

Endpoint Reporting in Medical Journals Needs to Be Revamped: Review

Michael O'Riordan

August 17, 2021

News Daily News

TCTMD’s Top 10 Most Popular Stories for March 2021

Shelley Wood

April 02, 2021

News Daily News

FDA Data Raise Red Flags for Suture-Based Vascular Closure Devices

Caitlin E. Cox

February 11, 2021

News Daily News

CMS Extends MitraClip Coverage to Functional MR, Carves Out Imager Role

Shelley Wood

January 20, 2021

News Daily News

Too Many HF Trial Results Underreported or Never Published

L.A. McKeown

June 23, 2020

News Conference News STS 2020

TAVR Tussle at US Surgery Meeting Threatens to Widen Surgeon-Cardiologist Wedge

Yael L. Maxwell

January 29, 2020

News Conference News AHA 2019

More Adverse Events, Higher Costs With Impella: New Observational Studies

Caitlin E. Cox

November 17, 2019

News Conference News VIVA 2019

Future Pulmonary Embolism Interventions: Wild West or Working Together?

L.A. McKeown

November 14, 2019

News Daily News

Public Comments Largely Supportive of CMS Plan for TAVR, With Some Suggested Tweaks

Todd Neale

May 01, 2019

News Daily News

Global Investigative Journalism Initiative Takes Aim at Medical Device Industry

Todd Neale

November 26, 2018

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Little Pre- and Postmarket Testing for Most Recalled CV Devices

Women, Black Patients Less Likely to Get Advanced PE Therapy, Analysis Shows

Women and Minorities Underrepresented in Heart Valve Trials

The More Tweaks Made to PMA-Approved Devices, the More Likely a Recall

RECORD4 Trial of Rivaroxaban, Published in 2009, Still Turning Heads

More Endpoints, More Problems: FDA Offers Advice for Multi-endpoint Trials

Most Patient-Reported Outcome Measures in CVD Fall Short

Postmarketing Studies of CV Devices Still Lacking in the US

Penumbra’s JET 7 Recall: A Kick Start to Change?

VASCADE Closure Device: FDA Database Tracks Common Complications, Deaths

Endpoint Reporting in Medical Journals Needs to Be Revamped: Review

TCTMD’s Top 10 Most Popular Stories for March 2021

FDA Data Raise Red Flags for Suture-Based Vascular Closure Devices

CMS Extends MitraClip Coverage to Functional MR, Carves Out Imager Role

Too Many HF Trial Results Underreported or Never Published

TAVR Tussle at US Surgery Meeting Threatens to Widen Surgeon-Cardiologist Wedge

More Adverse Events, Higher Costs With Impella: New Observational Studies

Future Pulmonary Embolism Interventions: Wild West or Working Together?

Public Comments Largely Supportive of CMS Plan for TAVR, With Some Suggested Tweaks

Global Investigative Journalism Initiative Takes Aim at Medical Device Industry

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