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News Daily News

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

Todd Neale

May 27, 2016

News Daily News

Another CV Outcomes Trial Testing Weight-Loss Drug Contrave Terminated Early

Michael O'Riordan

April 14, 2016

News Daily News

USPSTF 收紧一级预防的建议，称阿司匹林应只在高危人群中使用

Michael O'Riordan

April 12, 2016

News Daily News

Northwestern Memorial Hospital and Star CV Surgeon Found Not Guilty in Myxo Ring Case

Shelley Wood

April 08, 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

FDA Review of Absorb Bioresorbable Stent Does Not Tip Hand Ahead of Tomorrow’s Advisory Panel Meeting

Michael O'Riordan

March 14, 2016

News Daily News

Will FDA’s Settlement With Amarin Weaken Agency Oversight of Off-Label Promotion?

Michael O'Riordan

March 09, 2016

News Daily News

Controversial LIGHT Trial Now Published but Fails to Illuminate CV Risks of Contrave

Michael O'Riordan

March 08, 2016

News Daily News

Cardiologist Robert Califf Becomes New Commissioner of the FDA

L.A. McKeown

February 23, 2016

News Daily News

FDA: No Cardiovascular Event Reduction Claim for Ezetimibe

Shelley Wood

February 16, 2016

News Daily News

ROCKET AF Investigators: Problems With Warfarin Monitoring Device Did Not Skew Results

Todd Neale

February 04, 2016

News Daily News

FDA 的前职员表示，各抗血栓试验的缺失数据使得药物作用蒙上疑云

Shelley Wood

January 18, 2016

News Daily News

三大学会为实施 LAA 封堵手术的术者和机构提供建议

L.A. McKeown

December 10, 2015

News Daily News

Societies Issue Recommendations for Operators, Institutions Offering LAA Closure Procedures

L.A. McKeown

December 10, 2015

News Daily News

Las Sociedades Publican Recomendaciones para que Operadores y Centros Ofrezcan Intervenciones para el Cierre del AAI

L.A. McKeown

December 10, 2015

News Daily News

Path to Top FDA Post Gets a Bit Rockier for Califf

Michael O'Riordan

December 09, 2015

News Industry News

Amsel Medical Corporation Announces Filing of 2nd 510(k) Pre-Marketing Notification with the US Food and Drug Administration for the Amsel Occluder Device

October 27, 2015

News Daily News

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Yael L. Maxwell

July 17, 2015

News Daily News

Survival Benefit of CoreValve in High-Risk Patients Persists at 2 Years

July 07, 2015

News Daily News

Statement on LAA Closure Highlights Key Issues for Growing Field

July 02, 2015

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

Another CV Outcomes Trial Testing Weight-Loss Drug Contrave Terminated Early

USPSTF 收紧一级预防的建议，称阿司匹林应只在高危人群中使用

Northwestern Memorial Hospital and Star CV Surgeon Found Not Guilty in Myxo Ring Case

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

FDA Review of Absorb Bioresorbable Stent Does Not Tip Hand Ahead of Tomorrow’s Advisory Panel Meeting

Will FDA’s Settlement With Amarin Weaken Agency Oversight of Off-Label Promotion?

Controversial LIGHT Trial Now Published but Fails to Illuminate CV Risks of Contrave

Cardiologist Robert Califf Becomes New Commissioner of the FDA

FDA: No Cardiovascular Event Reduction Claim for Ezetimibe

ROCKET AF Investigators: Problems With Warfarin Monitoring Device Did Not Skew Results

FDA 的前职员表示，各抗血栓试验的缺失数据使得药物作用蒙上疑云

三大学会为实施 LAA 封堵手术的术者和机构提供建议

Societies Issue Recommendations for Operators, Institutions Offering LAA Closure Procedures

Las Sociedades Publican Recomendaciones para que Operadores y Centros Ofrezcan Intervenciones para el Cierre del AAI

Path to Top FDA Post Gets a Bit Rockier for Califf

Amsel Medical Corporation Announces Filing of 2nd 510(k) Pre-Marketing Notification with the US Food and Drug Administration for the Amsel Occluder Device

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Survival Benefit of CoreValve in High-Risk Patients Persists at 2 Years

Statement on LAA Closure Highlights Key Issues for Growing Field

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