Search - tctmd.com

Displaying 61 - 77 of 77

Sort: Relevancy | Date

News Industry News

Post-Market Study Evaluating The Boston Scientific Lotus™ Valve System Demonstrates Extremely Low PVL Rates

May 20, 2015

News Industry News

New Data Presented At EuroPCR 2015 Demonstrate Strong Performance Of The SYNERGY™ Bioabsorbable Polymer Stent System Over Four Years

May 19, 2015

News Industry News

REPRISE II Data Demonstrate Sustained Safety And Performance Outcomes At One Year For The Boston Scientific Lotus™ Valve System

September 15, 2014

News Daily News

Sapien XT Given Go-Ahead to Make US Debut

Caitlin E. Cox

June 24, 2014

News Daily News

Sapien XT Aprobado; Hará su Aparición en EE.UU.

Caitlin E. Cox

June 24, 2014

News Features

Interventionalists See Google Glass as the Next Frontier After Practical Issues Remedied

Yael L. Maxwell

June 13, 2014

News Daily News

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

L.A. McKeown

May 09, 2014

News Daily News

Cardiovascular Devices Make Up Largest Class of FDA Device Recalls Since 2005

Yael L. Maxwell

April 03, 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

TAVR Use Outstrips Evidence in Europe, BMJ Analysis Says

August 02, 2012

News Daily News

RACE: Regional STEMI Care System Improves Time to Reperfusion, Survival

Yael L. Maxwell

June 06, 2012

News Daily News

TAVR Travelers: Medical Tourism Gaining Ground

L.A. McKeown

September 26, 2011

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

Video

» On Record

On Record: Does Device Regulation Need More Crosstalk to Improve Access, Safety?

July 19, 2019

Advertisement

Post-Market Study Evaluating The Boston Scientific Lotus™ Valve System Demonstrates Extremely Low PVL Rates

New Data Presented At EuroPCR 2015 Demonstrate Strong Performance Of The SYNERGY™ Bioabsorbable Polymer Stent System Over Four Years

REPRISE II Data Demonstrate Sustained Safety And Performance Outcomes At One Year For The Boston Scientific Lotus™ Valve System

Sapien XT Given Go-Ahead to Make US Debut

Sapien XT Aprobado; Hará su Aparición en EE.UU.

Interventionalists See Google Glass as the Next Frontier After Practical Issues Remedied

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

Cardiovascular Devices Make Up Largest Class of FDA Device Recalls Since 2005

Regulatory Hurdles Pose Challenges for Device Approvals in US, Europe

TCT Leadership Outlines the State of Intervention

TAVR Use Outstrips Evidence in Europe, BMJ Analysis Says

RACE: Regional STEMI Care System Improves Time to Reperfusion, Survival

TAVR Travelers: Medical Tourism Gaining Ground

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

On Record: Does Device Regulation Need More Crosstalk to Improve Access, Safety?

Advertisement

Advertisement

Sign In

Forgot Your Password?

Search TCTMD

CME TITLE

Sign up for our newsletter

Search TCTMD

Submit an Event

Become a PREMIUM MEMBER or LOG IN to view exclusive content

REGISTER for free or LOG IN to view this content