News Daily News IVC Filter Lawsuits Expose Holes in FDA Oversight and Public Communication L.A. McKeown December 03, 2024
News Daily News Michelle Tarver Named New FDA Director of Medical Devices L.A. McKeown October 25, 2024
News Daily News Little Pre- and Postmarket Testing for Most Recalled CV Devices Michael O'Riordan September 16, 2024
News Daily News ‘Hey, ChatGPT: Surgery or the Cath Lab?’ Study Shows AI Can Aid Decision-Making Yael L. Maxwell August 14, 2024
News Daily News FDA Medical Devices Chief Jeff Shuren Announces Retirement L.A. McKeown July 24, 2024
News Daily News Two New Studies Highlight Lack of Diversity in Cardiovascular RCTs Michael O'Riordan July 11, 2023
News Daily News Medical Devices Cleared on Faulty Predicates More Likely to be Recalled Michael O'Riordan January 17, 2023
News Daily News Risk of Radiation Low for Pregnant Operators When Precautions Taken Michael O'Riordan September 27, 2022
News Daily News Most Clinical Trial Sponsors Fail to Report Data as Mandated by FDA Michael O'Riordan January 21, 2020
News Daily News STEMI Mortality Unaffected by Weekend, Weeknight, or Holiday Admission in France Michael O'Riordan October 31, 2019
News Daily News Acupuncture for Angina? Chinese Study Backs Targeted Approach Caitlin E. Cox July 31, 2019
News Daily News FDA Charts Path for ‘Resurrection’ of Device-Based Antihypertensive Therapies Michael O'Riordan December 06, 2018
News Daily News FDA Touts Increased Oversight of Medical Device Makers Michael O'Riordan November 22, 2018
News Daily News ‘The Bleeding Edge’ Documentary, Tackling Medical Device Regulation, Spurs Diverse Cardiology Reactions Yael L. Maxwell August 17, 2018
News Daily News High-Risk Medical Device Approval Process in Europe Inches Towards Transparency Michael O'Riordan July 20, 2018
News Daily News FDA Takes on 3-D Printing in Healthcare With Initial Guidance Document Yael L. Maxwell December 06, 2017
News Daily News ‘A Healthy Brexit’? How a Split From EU Could Affect UK Health System Yael L. Maxwell October 02, 2017
News Daily News FDA Clearance of Modified Devices Relies Heavily on Weak Studies, Surrogate Endpoints Michael O'Riordan August 16, 2017