Food

  • Read more: Jelly Beans, Booze, and B-Vitamins

    Jelly Beans, Booze, and B-Vitamins

    By Seán Finan The FDA’s policy guidelines on nutritional fortification include the so-called “jelly-bean rule:” the FDA considers it inappropriate to fortify candy or soda with nutrients because to do so would allow “misleading health claims” to be made about a putatively unhealthy product. Candy companies that tried to add vitamins their products to market…

  • Read more: Bold New Policies for The Brave New Biologies: IPRs and Innovation in Synthetic Biology and Gene editing

    Bold New Policies for The Brave New Biologies: IPRs and Innovation in Synthetic Biology and Gene editing

    Research Seminar at the University of Copenhagen debating intellectual property and innovation in synthetic biology, systems biology & gene editing. New technologies in biology offer a brave new world of possibilities. Promising solutions to some of the most urgent challenges faced by humanity: climate change, environmental protection, growing population, renewable energy and improved health care. Scientific…

  • Read more: George Annas on ‘The Week in Health Law’ Podcast

    George Annas on ‘The Week in Health Law’ Podcast

    By Nicolas Terry and Frank Pasquale This week we talked with George J. Annas, Chairman of the Bioethics & Human Rights Department, and William Fairfield Warren Distinguished Professor, at Boston University. George’s work is legendary among health policy experts; a 1998 tribute from Jay Katz gives some sense of its breadth and depth. Having reviewed numerous works, Katz states:”I have barely conveyed the…

  • Read more: New Food Law and Policy Clinic at UCLA Seeks Clinical Director

    New Food Law and Policy Clinic at UCLA Seeks Clinical Director

    The UCLA Resnick Program is launching a Food Law and Policy Clinic during the 2016-17 academic year.  The clinic’s programmatic mission will be to facilitate sufficient access to socially, economically, and environmentally sustainable food and to improve food environments particularly for low income populations and marginalized communities. To launch the clinic, we are seeking a…

  • Read more: FDA’s Relationship with Marijuana: It’s Complicated

    FDA’s Relationship with Marijuana: It’s Complicated

    By Elizabeth Guo Marijuana and marijuana-derived products are top of mind for state legislatures these days. On March 10, the Virginia state legislature passed a bill legalizing cannabidiol oil, a marijuana-derived product, for patients who suffer from epilepsy. Other legislatures are actively debating measures to legalize cannabis-related products in their states, and many of these…

  • Read more: Minnesota: Leading The Way In Patient Safety

    Minnesota: Leading The Way In Patient Safety

    By John Tingle The UK Government and the Department of Health are taking patient safety very seriously and, since the publication of ‘An organisation with a memory’ in 2000, the UK has like the USA been a world leader in the field of patient safety policies, practices and developments. In the UK we have a…

  • Read more: The FDA de-regulates the first genetically-engineered animal

    The FDA de-regulates the first genetically-engineered animal

    By Joanna Sax On November 19, 2015, the FDA de-regulated the AquAdvantage Salmon.  This salmon is genetically engineered to grow faster.  This is the first time the FDA has de-regulated a genetically engineered animal. Let me just say from the outset that the scientific consensus is clear that genetically engineered food is as safe as…

  • Read more: Introducing New Blogger Peng Zhao

    Introducing New Blogger Peng Zhao

    The Petrie-Flom Center is pleased to welcome Visiting Scholar Peng Zhao to the Bill of Health as our newest contributor, who will blog primarily about China’s drug and food law and regulatory policy. Peng Zhao earned his BA (2003), MA (2009), and PhD (2009) in law from the China University of Political Science and Law (CUPL, Beijing). He serves…

  • Read more: Does FDA Need a Dietary Supplement User Fee Act?

    Does FDA Need a Dietary Supplement User Fee Act?

    By Elizabeth Guo Dietary supplements are dominating headlines these days – and not in a good way. Last Wednesday, Nevada officials found basketball star Lamar Odom unconscious at a brothel after taking cocaine along , a sexual enhancement dietary supplement. That same week, the New England Journal of Medicine released an article finding that dietary…

  • Read more: The FDA’s Determination On Artificial Trans Fat: A Long Time Coming

    The FDA’s Determination On Artificial Trans Fat: A Long Time Coming

    By Diana R. H. Winters [cross-posted at Health Affairs Blog]On June 16, 2015, the Food and Drug Administration (FDA) released its final determination withdrawing the generally recognized as safe (GRAS) designation for partially hydrogenated oils (PHOs), which are the main source of artificial trans fat in processed foods. The agency gave the food industry three…