News Daily News The Hornet’s Nest of Data Sharing: Cardiologist-Led Proposals Do Not Necessarily Agree on Timelines, Reviews Shelley Wood August 03, 2016
News Daily News Medical Devices Approved More Quickly in EU Face More Safety Alerts and Recalls Shelley Wood July 05, 2016
News Daily News ¿Está Cerca el Fin de los Exámenes de Re-certificación? ABIM Anuncia una 2ª Opción de Evaluación en Casa Yael L. Maxwell May 09, 2016
News Daily News Is the End of Recertification Exams Near? ABIM Announces At-Home Assessment Option Yael L. Maxwell May 09, 2016
News Daily News More Studies of Investigational High-Risk Cardiovascular Devices are Getting Published Shelley Wood March 02, 2016
News Daily News Cardiologist Robert Califf Becomes New Commissioner of the FDA L.A. McKeown February 23, 2016
News Daily News Years Later, Myxo Ring Controversy Heads to Courts, Taking on Northwestern Memorial and Star CV Surgeon Shelley Wood February 11, 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 ABIM Prolongs Decision to Suspend Certain MOC Modules Yael L. Maxwell December 20, 2015
News Daily News It’s Official: Europe Bans Direct Industry Sponsorship of Physicians for CME Todd Neale December 02, 2015
News Daily News FDA Warns of Potentially Serious Problems With Intravascular Device Coatings Shelley Wood November 22, 2015
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 One-Quarter of Diagnostic CAD Catheterizations Deemed Inappropriate in NY State Jason Kahn February 26, 2014
News Daily News Study Looks at Differences in PCI Outcomes at Teaching vs. Non-Teaching Hospitals Yael L. Maxwell August 12, 2013
News Daily News Large-Scale PCI Outcomes Study Shows Improvements Over Time in United States August 02, 2013
News Daily News Los Criterios del BARC Validados frente a las Definiciones Hemorrágicas Existentes Leah Lawrence March 23, 2012
News Daily News Report on Device Recalls Criticizes Current FDA Approval Process L.A. McKeown February 14, 2011