Carmel Shachar's guest appearances

Carmel Shachar

The Week in Health Law

Leo Beletsky

Nathan Cortez

Nicole Huberfeld

Nicholas Bagley

Elizabeth Leonard

Scott Burris

Christy Ford Chapin

Thad Pope

Wendy Parmet

Sylvester Stallone

John Cogan

Ross Silverman

Alexandra Phelan

Sam Halabi

Aaron Kesselheim

OwlTail

Barbara Evans

Nicholson Price

Craig Konnoth

Anthony P. Weiss

This is the second of three episodes of “Innovation and Protection: The Future of Medical Device Regulation,” a podcast miniseries created to replace the 2020 Petrie-Flom Center Annual Conference in light of the COVID-19 pandemic. These episodes highlight a selection of papers that were written for the conference, which was organized in collaboration with the University of Copenhagen’s Center for Advanced Studies in Biomedical Innovation Law (CeBIL) and the University of Arizona Health Law Program. All of the papers will be published in an edited volume. First, Nicholson Price, Professor at the University of Michigan School of Law, interviews Craig Konnoth, Associate Professor of Law at University of Colorado-Boulder School of Law, about his paper, “Are Electronic Health Records Medical Devices?” Next, Petrie-Flom Center Executive Director Carmel Shachar and Anthony P. Weiss, Senior Vice President and Chief Medical Officer at the Beth Israel Deaconess Medical Center, discuss his paper, “Professional Self-Regulation in Medicine: Will the Rise of Intelligent Tools Mean the End of Peer Review?” Then Price returns to talk with Barbara Evans, Mary Ann &amp; Lawrence E. Faust Professor of Law at the University of Houston Law Center, about “Product Liability Risks and Defenses for FDA-Regulated AI/ML Software.”

214. Technological Advancements & Medical Device Regulation. Guests, Nicholson Price, Craig Konnoth, Carmel Shachar, Anthony P. Weiss, and Barbara Evans.

Glen Cohen

Matthew Herder

Christoper Robertson

This is the first of three episodes of “Innovation and Protection: The Future of Medical Device Regulation,” a podcast miniseries created to replace the 2020 Petrie-Flom Center Annual Conference in light of the COVID-19 pandemic. These episodes highlight a selection of papers that were written for the conference, which was organized in collaboration with the University of Copenhagen’s Center for Advanced Studies in Biomedical Innovation Law (CeBIL) and the University of Arizona Health Law Program. All of the papers will be published in an edited volume. This first episode looks at big-picture issues with medical device regulation in the U.S. First, Petrie-Flom Center Faculty Director I. Glenn Cohen interviews Matthew Herder, Director of the Health Law Institute at the Schulich School of Law at Dalhousie University to discuss his paper, “A 'DESI' Designed for Devices: Insights from the FDA's Drug Efficacy Study Implementation program initiated during the 1960s for the improved regulation of medical devices today.” Then Petrie-Flom Center Executive Director Carmel Shachar talks with Efthimios Parasidis, Professor of Law and Public Health at Ohio State University about “Compulsory Medical Device Registries: Legal and Ethical Issues.” Last, Christopher Robertson discusses “Crisis Equals Opportunity and Danger: The opioid epidemic, problem-solving courts, and the manufacture of a new medical device market,” with author Ross Silverman, professor at Indiana University’s School of Public Health.

211. Future of Medical Device Regulation. Guests, Carmel Shachar, Glen Cohen, Matthew Herder, Christoper Robertson, and Ross Silverman.