In a previous blog post, we detailed the regulation for the labeling of genetically modified organisms (GMOs) and bioengineered (BE) foods under the new National Bioengineered Food Disclosure Standard (NBFDS) in the United States. You may think that the terms of the law are black and white – if a GMO is present in your product, you need to declare its presence on your food label under new regulations. However, as with most things in life, there is a distinct grey area. To uncomplicate the regulations, we put together a guide to understanding the GMO labeling guidelines and the exemptions that may apply to your products. Continue Reading
Over the last 30 years, the debate over bioengineered foods – specifically, the boom in Genetically Modified Organisms (GMOs) – has grown from a quiet dialogue to a wide-spread, boisterous debate. Most recently, issues around disclosure and forthcoming U.S. regulations have taken center stage.
In order to leverage burgeoning new markets in what I call the “progressive food movement,” an increasing number of companies are accessorizing their food labels with new non-GMO claims. Now, a new federal law, called the National Bioengineered Food Disclosure Standard (NBFDS), will require food manufacturers to disclose the use of GMO ingredients in their products. Of course, the current draft of the regulations can be a bit confusing, often vague and have wide-ranging implications that vary from business to business. Continue Reading
Food industry associations and consumer advocacy groups have influenced the development of many key U.S. food policies and regulations, but the impact of consumer lawsuits upon the regulatory process cannot be denied. Since 2008, the number of class action lawsuits filed against food and beverage companies has increased from approximately twenty to more than a hundred lawsuits annually in recent years. While some of the legal challenges could be dismissed as frivolous, several cases have fueled the evolution of significant labeling and safety regulatory initiatives that are now under consideration by the U.S. Food and Drug Administration (FDA). Continue Reading
I’ll be honest – from time to time, I enjoy throwing on my teal yoga pants and visiting my favorite organic supermarket. I love perusing the endless rows of organic and otherwise non-Genetically Modified Organism (non-GMO) products adorning shelf upon shelf. With all of those “verified” and “certified” products smiling down at me, how can I not smile back? After all, like many shoppers, I place my trust in progressive statements on food labels, such as “Organic,” “non-GMO,” “Fair Trade,” “Hormone-Free,” “Allergen-Free,” and the list goes on. Before I leave the store, my cart is adorned with at least three or four items bearing one of these claims. Continue Reading
Writer G.K. Chesterton once suggested that, “Whenever you remove any fence, always pause long enough to ask why it was put there in the first place.” This advice seems particularly relevant to the current deregulatory environment in the United States. A 2017 Executive Order required federal agencies to eliminate two regulations for every new regulation, which resulted in the withdrawal or delay of 1,579 regulations. How might the removal of positive regulatory initiatives impact food safety, public health and your business in the new year? Continue Reading