Events with Recording

  • Read more: Third Annual Health Law Year in P/Review
    Jan 30

    Third Annual Health Law Year in P/Review

    Couldn’t make it in person? Check out the individual sessions in the videos linked above and the collaborative blog series on the Health Affairs Blog (links below)! The Third Annual Health Law Year in P/Review symposium featured leading experts discussing major developments during 2014 and what to watch out for in 2015. The discussion at…

  • Read more: A “Natural” Experiment
    Jan 29

    A “Natural” Experiment

    Consumer Confusion and Food Claims, a lecture by Efthimios Parasidis Video of the lecture and following discussion is available online. What makes food “natural”? Do consumers understand “natural” claims on food labels? In the absence of robust federal guidelines, are state laws or class action lawsuits appropriate mechanisms for addressing false or misleading “natural” claims?…

  • Read more: Outbreak: Developing New Medical Products for Epidemics,
    Jan 15

    Outbreak: Developing New Medical Products for Epidemics,

    A lecture by Peter Hutt Video of the lecture and following discussion are available online. The recent outbreak of Ebola has called attention to the substantial difficulties associated with developing and testing new products for time-sensitive epidemics. What are the legal, ethical, and economic barriers to getting essential treatments and preventative measures from the lab…

  • Read more: Book Launch: Patients with Passports: Medical Tourism, Law, and Ethics
    Nov 19

    Book Launch: Patients with Passports: Medical Tourism, Law, and Ethics

    I. Glenn Cohen‘s new book Patients with Passports: Medical Tourism, Law, and Ethics (Oxford University Press, 2014) is the first comprehensive legal and ethical analysis of medical tourism. Examining both the legal and ethical issues raised by medical tourism and how the two interact, it provides the best currently available data and explanations of the…

  • Read more: Law and Ethics of Non-Invasive Prenatal Testing
    Nov 6

    Law and Ethics of Non-Invasive Prenatal Testing

    The Petrie-Flom Center hosted a discussion of the issues surrounding noninvasive prenatal testing (NIPT), a screening method for detecting certain specific chromosomal abnormalities, as well as sex, in utero. NIPT may help mothers avoid other tests that could put their pregnancies at risk, but the ability to detect substantial information about a developing fetus with…

  • Read more: Global Reproduction
    Nov 5

    Global Reproduction

    Health, Law, and Human Rights in Surrogacy and Egg Donation A screening of the documentary Can We See the Baby Bump, Please?, which was followed by a panel discussion of the legal and human rights issues surrounding surrogacy and egg donation in a global context. The film screening began at 5PM, followed by the panel…

  • Read more: Human Subjects Research Regulation: Perspectives on the Future
    Oct 22

    Human Subjects Research Regulation: Perspectives on the Future

    MIT Press recently published Human Subjects Research Regulation: Perspectives on the Future (2014), co-edited by Petrie-Flom Center Faculty Director, I. Glenn Cohen, and Executive Director, Holly Fernandez Lynch. This edited volume stems from the Center’s 2012 annual conference, which brought together leading experts in a conversation about whether and how the current system of human…

  • Read more: Legal and Ethical Issues in Healthcare Start-Ups
    Oct 6

    Legal and Ethical Issues in Healthcare Start-Ups

    (followed by Petrie-Flom’s 2014 Open House) New healthcare start-ups face a range of legal and ethical challenges as they develop new products and services and solicit financial support from investors. Building on the success of the President’s Challenge at the Harvard Innovation Lab, which invites teams of Harvard students to develop innovative solutions to a…

  • Read more: A Conversation with the HHS Office of the Inspector General
    Sep 30

    A Conversation with the HHS Office of the Inspector General

    A conversation with the Boston office of the U.S. Department of Health and Human Services Office of the Inspector General (OIG), Office of Evaluation and Inspections. The OIG has for decades served as the foremost government watchdog of federal healthcare programs, overseeing Medicare, Medicaid, the Food and Drug Administration, the National Institutes of Health, and…

  • Read more: Post-Trial Responsibilities
    Sep 18

    Post-Trial Responsibilities

    Ethics and Implementation Conference Description Who: Clinical research sponsors, investigators, funders, regulators, trial participants, and other stakeholders Introduction / Background: The term “post-trial access” is used broadly to connote a wide range of possibilities for providing continued access to study interventions (and potentially other care) once a trial is over, or a subject’s participation has…