Matthew Herder's guest appearances

Matthew Herder

The Week in Health Law

Law Bytes

Leo Beletsky

Eric Goldman

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

OwlTail

Bill C-13, the COVID-19 Emergency Response Act, was the Canadian government’s legislative response to the Coronavirus pandemic. In addition a host of economic measures, the bill included some unexpected patent law provisions designed to speed access to essential medicines, devices or treatments. Matthew Herder, the director of the Health Law Institute at Dalhousie University, joins the podcast discuss the new Canadian rules, the use of compulsory licensing to enhance access to medicines, and other innovative approaches to overcoming potential access barriers raised by intellectual property laws. The podcast can be downloaded here and is embedded below. Subscribe to the podcast via Apple Podcast, Google Play, Spotify or the RSS feed. Updates on the podcast on Twitter at @Lawbytespod.  Credits: CTV News, Canada’s Chief Public Health Officer Says a Coronavirus Vaccine is ‘Probably’ a Year Away

Bill C-13, the <a href="https://www.parl.ca/DocumentViewer/en/43-1/bill/C-13/royal-assent" rel="nofollow" target="_blank">COVID-19 Emergency Response Act</a>, was the Canadian government’s legislative response to the Coronavirus pandemic. In addition a host of economic measures, the bill included some unexpected patent law provisions designed to speed access to essential medicines, devices or treatments. <a href="https://www.dal.ca/faculty/law/faculty-staff/our-faculty/matthew-herder.html" rel="nofollow" target="_blank">Matthew Herder</a>, the director of the Health Law Institute at Dalhousie University, <a href="https://episodes.castos.com/lawbytes/Ep.-46-Herder.mp3" rel="nofollow" target="_blank">joins the podcast</a> discuss the new Canadian rules, the use of compulsory licensing to enhance access to medicines, and other innovative approaches to overcoming potential access barriers raised by intellectual property laws. The podcast can be <a href="https://episodes.castos.com/lawbytes/Ep.-46-Herder.mp3" rel="nofollow" target="_blank">downloaded here</a> and is embedded below. Subscribe to the podcast via <a href="https://itunes.apple.com/ca/podcast/law-bytes/id1455262794?mt=2" rel="nofollow" target="_blank">Apple Podcast</a>, <a href="https://playmusic.app.goo.gl/?ibi=com.google.PlayMusic&amp;isi=691797987&amp;ius=googleplaymusic&amp;apn=com.google.android.music&amp;link=https://play.google.com/music/m/Iaqrcdxptdr55qq7eilrtjrmubu?t%3DLawBytes%26pcampaignid%3DMKT-na-all-co-pr-mu-pod-16" rel="nofollow" target="_blank">Google Play</a>, <a href="https://open.spotify.com/show/5iDUCcDrkzGai0OdTgoucv?si=IZc4-lCCQ4GlyoHEo16wdA" rel="nofollow" target="_blank">Spotify</a> or the <a>RSS feed</a>. Updates on the podcast on Twitter at <a href="https://twitter.com/lawbytespod" rel="nofollow" target="_blank">@Lawbytespod</a>. Credits: <a href="https://www.youtube.com/watch?v=V4NalJYQr-Q" rel="nofollow" target="_blank">CTV News, Canada’s Chief Public Health Officer Says a Coronavirus Vaccine is ‘Probably’ a Year Away</a>

Episode 46: Matthew Herder on the Canadian Effort to Break Down Patent Barriers to Accessing Coronavirus Medicines

Carmel Shachar

Glen Cohen

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.