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News Daily News

Two New Studies Highlight Lack of Diversity in Cardiovascular RCTs

Michael O'Riordan

July 11, 2023

News Daily News

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

Michael O'Riordan

October 28, 2022

News Daily News

Dobutamine Shortage: ACC Experts Offer Tips, Alternatives

Shelley Wood

August 11, 2022

News Daily News

USPSTF: Most Vitamin, Supplement Data Still ‘Inconclusive’ on CVD Benefits

Yael L. Maxwell

June 23, 2022

News Features TVT 2022

Minorities, Poorer Patients Missing Out on Structural Heart Care

Michael O'Riordan

June 15, 2022

News Daily News

Skipping Low-Value Cardiovascular Care Could Save Billions: AHA

Michael O'Riordan

March 01, 2022

News Daily News

FDA Issues New Guidance on Sodium Targets for Food Industry

L.A. McKeown

October 14, 2021

News Features

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

Michael O'Riordan

December 17, 2020

News Daily News

Payments to Docs Appear to Influence Implantable Device Selection

Michael O'Riordan

November 04, 2020

News Conference News CRT 2020

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

Michael O'Riordan

February 28, 2020

News Conference News CRT 2020

Positive Early Data for TAVR in Low-Risk Patients With Bicuspid Valves

Michael O'Riordan

February 27, 2020

News Daily News

ACC/AHA Guideline Writers’ Disclosures vs Open Payments Don’t Add Up

Caitlin E. Cox

December 05, 2019

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

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

Yael L. Maxwell

December 06, 2017

News Daily News

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

Todd Neale

May 27, 2016

News Daily News

Cardiologist Robert Califf Becomes New Commissioner of the FDA

L.A. McKeown

February 23, 2016

News Daily News

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

Caitlin E. Cox

January 03, 2016

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

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Two New Studies Highlight Lack of Diversity in Cardiovascular RCTs

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

Dobutamine Shortage: ACC Experts Offer Tips, Alternatives

USPSTF: Most Vitamin, Supplement Data Still ‘Inconclusive’ on CVD Benefits

Minorities, Poorer Patients Missing Out on Structural Heart Care

Skipping Low-Value Cardiovascular Care Could Save Billions: AHA

FDA Issues New Guidance on Sodium Targets for Food Industry

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

Payments to Docs Appear to Influence Implantable Device Selection

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

Positive Early Data for TAVR in Low-Risk Patients With Bicuspid Valves

ACC/AHA Guideline Writers’ Disclosures vs Open Payments Don’t Add Up

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

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

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

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

Cardiologist Robert Califf Becomes New Commissioner of the FDA

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

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

Regulatory Hurdles Pose Challenges for Device Approvals in US, Europe

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