News Conference News TCT 2023 Some Surprises in Low-Risk TAVI Follow-up: PARTNER 3 and Evolut Trials Michael O'Riordan October 24, 2023
News Daily News US, European Hypertension Guidelines: More Alike Than Different Caitlin E. Cox August 17, 2022
News Conference News SCAI 2022 SCAI PFO Closure Guideline Addresses Real-world Patient Scenarios L.A. McKeown May 20, 2022
News Conference News SCCT 2020 Biggest Barriers to Cardiac CT? Old Myths, Fair Payment, and De-adoption Yael L. Maxwell July 22, 2020
News Daily News High-Risk Medical Device Approval Process in Europe Inches Towards Transparency Michael O'Riordan July 20, 2018
News Daily News USPSTF: Insufficient Evidence to Support CAC Score, hsCRP, or ABI for Risk Assessment Michael O'Riordan July 12, 2018
News Daily News Medical Devices Approved More Quickly in EU Face More Safety Alerts and Recalls Shelley Wood July 05, 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 Proposal Seeks to Shine Early Spotlight on Postmarket Device Safety Concerns Caitlin E. Cox January 03, 2016
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 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