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News Daily News

SCAI/HRS Issue First Practice Guideline for LAAO

Yael L. Maxwell

August 06, 2025

News Daily News

Coverage and Use of Impella and Watchman: A Tale of Four Countries

Michael O'Riordan

March 04, 2025

News Conference News STS 2024

TAVI, SAVR Almost Equally Performed in California Patients Under 60

Yael L. Maxwell

February 01, 2024

News Daily News

No Safety Concerns Seen With Inclisiran in Large ORION Analysis

Michael O'Riordan

December 06, 2023

News Daily News

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

Michael O'Riordan

October 28, 2022

News Features

Novel Targets, Gene Edits, and Vaccines: Is a ‘Golden Era’ Dawning for ASCVD?

Michael O'Riordan

August 15, 2022

News Daily News

British Medical Groups Express Concern About Inclisiran Rollout

Michael O'Riordan

December 14, 2021

News Conference News EACTS 2021

TAVI Registries Offer Outcome Clues as Low-Risk Numbers Climb

Shelley Wood

October 20, 2021

News Daily News

USPSTF at Last Takes Tougher Stance on Aspirin in Primary Prevention

Shelley Wood

October 15, 2021

News Features

Funding the Future: How Industry Support for CV Trials Could Evolve

Michael O'Riordan

December 17, 2020

News Conference News CRT 2020

Newer, Thinner-Strut Abbott Scaffold Prompts Talk of a BVS Comeback

Michael O'Riordan

February 28, 2020

News Daily News

Interventional Options and Future Directions for Acute PE: New AHA Statement

Todd Neale

October 07, 2019

News Daily News

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

Michael O'Riordan

July 20, 2018

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

好人、坏人，还是大资金？业界施压要求将患者索赔数据与设备结局相关联

Shelley Wood

March 17, 2016

News Daily News

Good Guys, Bad Guys, or Just Big Money? The Push to Link Patient-Claims Data to Device Outcomes

Shelley Wood

March 17, 2016

News Daily News

关于实验性高危心血管装置的研究越来越多

Shelley Wood

March 02, 2016

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SCAI/HRS Issue First Practice Guideline for LAAO

Coverage and Use of Impella and Watchman: A Tale of Four Countries

TAVI, SAVR Almost Equally Performed in California Patients Under 60

No Safety Concerns Seen With Inclisiran in Large ORION Analysis

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

Novel Targets, Gene Edits, and Vaccines: Is a ‘Golden Era’ Dawning for ASCVD?

British Medical Groups Express Concern About Inclisiran Rollout

TAVI Registries Offer Outcome Clues as Low-Risk Numbers Climb

USPSTF at Last Takes Tougher Stance on Aspirin in Primary Prevention

Funding the Future: How Industry Support for CV Trials Could Evolve

Newer, Thinner-Strut Abbott Scaffold Prompts Talk of a BVS Comeback

Interventional Options and Future Directions for Acute PE: New AHA Statement

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

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

好人、坏人，还是大资金？业界施压要求将患者索赔数据与设备结局相关联

Good Guys, Bad Guys, or Just Big Money? The Push to Link Patient-Claims Data to Device Outcomes

关于实验性高危心血管装置的研究越来越多

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