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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

Un Panel Asesor de la FDA Recomienda por un Estrecho Margen una Indicación de Mortalidad por EAC para el Antidiabético Empagliflozina

Michael O'Riordan

June 30, 2016

News Daily News

FDA 顾问小组小范围建议使用糖尿病药物 empagliflozin 来改善 CVD 死亡率

Michael O'Riordan

June 30, 2016

News Daily News

FDA Advisory Panel Narrowly Recommends CVD Mortality Indication for Diabetes Drug Empagliflozin

Michael O'Riordan

June 30, 2016

News Daily News

Proposed Legislation Could Mandate Physician Reporting of Adverse Events With Medical Devices

Yael L. Maxwell

June 14, 2016

News Daily News

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

Todd Neale

May 27, 2016

News Daily News

Majority of FDA Advisors Give Green Light to Amplatzer PFO Closure Device for Stroke

Shelley Wood

May 25, 2016

News Daily News

US and European Heart Failure Guidelines Advocate Use of Two New Therapies

L.A. McKeown

May 24, 2016

News Daily News

Sluggish CMS Reimbursement Lags Cardiac Device Approvals: Should Value Endpoints be Added to Trials?

Yael L. Maxwell

May 02, 2016

News Daily News

No More Niacin, Fibrate Combinations With Statins: FDA

Michael O'Riordan

April 19, 2016

News Daily News

Former FDA Staffer Says Missing Data Across Antithrombotic Trials Cast Doubt on Drug Effects

Shelley Wood

January 18, 2016

News Daily News

Residual Dissection After DCB Treatment for De Novo CAD Generally Resolves

Caitlin E. Cox

November 26, 2015

News Daily News

Good News, Bad News Week for Watchman LAA Occluder

Shelley Wood

November 12, 2015

News Daily News

MVARC Document Offers Template for Mitral Valve Therapeutics Research

Todd Neale

July 16, 2015

News Daily News

Method Chosen to Estimate Pre-PCI Kidney Function Matters

L.A. McKeown

June 29, 2015

News Daily News

FDA Approves 2 New TAVR Systems for High-Risk, Inoperable Patients

Yael L. Maxwell

June 24, 2015

News Daily News

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

Yael L. Maxwell

April 03, 2014

News Daily News

Endovascular Treatment of Stroke, Though Uncommon, Gains Ground

Caitlin E. Cox

September 18, 2012

News Daily News

FDA, CMS Parallel Review Aims to Speed Access to Innovative Technologies

L.A. McKeown

October 14, 2011

News Daily News

Commentary Authors Urge Improvements to Device Approval Process

Caitlin E. Cox

July 20, 2011

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Los Dispositivos Médicos Aprobados Más Rápidamente en la UE son Objeto de Más Alertas de Seguridad y Nuevas Inspecciones

Un Panel Asesor de la FDA Recomienda por un Estrecho Margen una Indicación de Mortalidad por EAC para el Antidiabético Empagliflozina

FDA 顾问小组小范围建议使用糖尿病药物 empagliflozin 来改善 CVD 死亡率

FDA Advisory Panel Narrowly Recommends CVD Mortality Indication for Diabetes Drug Empagliflozin

Proposed Legislation Could Mandate Physician Reporting of Adverse Events With Medical Devices

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

Majority of FDA Advisors Give Green Light to Amplatzer PFO Closure Device for Stroke

US and European Heart Failure Guidelines Advocate Use of Two New Therapies

Sluggish CMS Reimbursement Lags Cardiac Device Approvals: Should Value Endpoints be Added to Trials?

No More Niacin, Fibrate Combinations With Statins: FDA

Former FDA Staffer Says Missing Data Across Antithrombotic Trials Cast Doubt on Drug Effects

Residual Dissection After DCB Treatment for De Novo CAD Generally Resolves

Good News, Bad News Week for Watchman LAA Occluder

MVARC Document Offers Template for Mitral Valve Therapeutics Research

Method Chosen to Estimate Pre-PCI Kidney Function Matters

FDA Approves 2 New TAVR Systems for High-Risk, Inoperable Patients

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

Endovascular Treatment of Stroke, Though Uncommon, Gains Ground

FDA, CMS Parallel Review Aims to Speed Access to Innovative Technologies

Commentary Authors Urge Improvements to Device Approval Process

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