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Antiguo Miembro de la FDA Dice que los Datos que Faltan sobre Ensayos Antitrombóticos arrojan una Sombra sobre los Efectos del Fármaco

Shelley Wood

January 18, 2016

News Daily News

FDA Grants Go-Ahead for Low-Risk TAVR Study

Shelley Wood

January 14, 2016

News Industry News

Edwards Receives FDA Approval For Expanded Indication Study Of SAPIEN 3 Valve

January 14, 2016

News Industry News

Neovasc Receives FDA Approval to add 40mm Valve Size to the TIARA-I Clinical Trial

January 10, 2016

News Industry News

Vascular Dynamics’ MobiusHD™ System Receives CE Mark for the Treatment of Resistant Hypertension

January 05, 2016

News Daily News

Sapien 是经导管肺动脉瓣置换的“可行、持久”方案

Michael O'Riordan

December 27, 2015

News Daily News

Sapien a ‘Viable and Durable’ Option in Transcatheter Pulmonary Valve Replacement

Michael O'Riordan

December 27, 2015

News Daily News

La Sapien es una Opción ‘Viable y Duradera’ en la Sustitución Transcatéter de la Válvula Pulmonar

Michael O'Riordan

December 27, 2015

News Daily News

Year in Review: Physicians Select the Most Important News of 2015, in Interventional Cardiology and Beyond

December 23, 2015

News Industry News

FDA Approves BIOTRONIK Iperia ICD Systems with Full-Body ProMRI Technology

December 21, 2015

News Industry News

FDA approves wearable defibrillator for children at risk for sudden cardiac arrest

December 17, 2015

News Daily News

LAAO Registry Launched to Track ‘Real-World’ Outcomes With Left Atrial Appendage Closure Procedures

Caitlin E. Cox

December 15, 2015

News Industry News

First Patients Enrolled in the Gore RELINE MAX Clinical Study

December 15, 2015

News Daily News

Ezetimibe Fails to Garner Support for CV- Event Reduction Claim From FDA Advisory Committee

Michael O'Riordan

December 15, 2015

News Daily News

美国政府审议对人类受试者研究规则的变更

Caitlin E. Cox

December 13, 2015

News Daily News

US Government Mulls Changes to Rules for Research in Humans

Caitlin E. Cox

December 13, 2015

News Daily News

El Gobierno de EE.UU. Medita Hacer Cambios a la Normativa sobre Investigación en Seres Humanos

Caitlin E. Cox

December 13, 2015

News Daily News

Societies Issue Recommendations for Operators, Institutions Offering LAA Closure Procedures

L.A. McKeown

December 10, 2015

News Daily News

Report Provides Snapshot of Initial Commercial TAVR Experience

Todd Neale

November 30, 2015

News Industry News

Boston Scientific Receives FDA Approval And CE Mark For AngioJet™ ZelanteDVT™ Thrombectomy Catheter

November 30, 2015

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Antiguo Miembro de la FDA Dice que los Datos que Faltan sobre Ensayos Antitrombóticos arrojan una Sombra sobre los Efectos del Fármaco

FDA Grants Go-Ahead for Low-Risk TAVR Study

Edwards Receives FDA Approval For Expanded Indication Study Of SAPIEN 3 Valve

Neovasc Receives FDA Approval to add 40mm Valve Size to the TIARA-I Clinical Trial

Vascular Dynamics’ MobiusHD™ System Receives CE Mark for the Treatment of Resistant Hypertension

Sapien 是经导管肺动脉瓣置换的“可行、持久”方案

Sapien a ‘Viable and Durable’ Option in Transcatheter Pulmonary Valve Replacement

La Sapien es una Opción ‘Viable y Duradera’ en la Sustitución Transcatéter de la Válvula Pulmonar

Year in Review: Physicians Select the Most Important News of 2015, in Interventional Cardiology and Beyond

FDA Approves BIOTRONIK Iperia ICD Systems with Full-Body ProMRI Technology

FDA approves wearable defibrillator for children at risk for sudden cardiac arrest

LAAO Registry Launched to Track ‘Real-World’ Outcomes With Left Atrial Appendage Closure Procedures

First Patients Enrolled in the Gore RELINE MAX Clinical Study

Ezetimibe Fails to Garner Support for CV- Event Reduction Claim From FDA Advisory Committee

美国政府审议对人类受试者研究规则的变更

US Government Mulls Changes to Rules for Research in Humans

El Gobierno de EE.UU. Medita Hacer Cambios a la Normativa sobre Investigación en Seres Humanos

Societies Issue Recommendations for Operators, Institutions Offering LAA Closure Procedures

Report Provides Snapshot of Initial Commercial TAVR Experience

Boston Scientific Receives FDA Approval And CE Mark For AngioJet™ ZelanteDVT™ Thrombectomy Catheter

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