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Plos Medicine|August 23, 2012
How does medical device regulation perform in the United States and the European union? A systematic reviewDaniel B Kramer, Shuai Xu, Aaron S KesselheimThe Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|March 8, 2023
The Right to Repair Software-Dependent Medical DevicesLars Lindgren, Aaron S Kesselheim, Daniel B KramerJAMA|January 23, 2014
FDA approval of cardiac implantable electronic devices via original and supplement premarket approval pathways, 1979-2012Benjamin N Rome, Daniel B Kramer, Aaron S KesselheimCurrent Cardiology Reports|April 25, 2014
Approval of high-risk medical devices in the US: implications for clinical cardiologyBenjamin N Rome, Daniel B Kramer, Aaron S KesselheimNature Biomedical Engineering|June 29, 2019
Review times and adverse events for cardiovascular devicesAriel Dora Stern, Daniel B Kramer, Melissa Ouellet, et al.Heart Rhythm|July 24, 2010
Ethical and legal views of physicians regarding deactivation of cardiac implantable electrical devices: a quantitative assessmentDaniel B Kramer, Aaron S Kesselheim, Dan W Brock, et al.The American Journal of Cardiology|February 8, 2011
Ethical and legal views regarding deactivation of cardiac implantable electrical devices in patients with hypertrophic cardiomyopathyDaniel B Kramer, Aaron S Kesselheim, Lisa Salberg, et al.Journal of the American Heart Association|August 22, 2019
Landscape of Cardiovascular Device Registries in the United StatesPrashant V Rajan, Jessica N Holtzman, Aaron S Kesselheim, et al.The Milbank Quarterly|September 22, 2011
An empirical review of major legislation affecting drug development: past experiences, effects, and unintended consequencesAaron S KesselheimThe Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|March 4, 2024
Government Support of Meaningful Drug and Device Innovation: Pathways and ChallengesAaron S KesselheimPageof 61