The U.S. Food and Drug Administration (FDA) is finally getting around to finalizing proposed rules implementing the Food Safety Modernization Act (FSMA), which was signed into law in 2011. Rules regarding preventive controls for human and animal food were recently finalized, and rules affecting produce safety and food imports are just around the corner. Compliance with the rules must be achieved as early as one year from now, depending on the particular rule and the size of your business. Continue reading
The Obama Administration’s recent budget proposal for FY 2016 endorsed the concept of establishing a single federal food safety agency—reviving discussion on what has been a long-standing issue. This initiative has generated many of the same talking points that have surrounded this topic for decades, including everyone’s favorite reference to the absurdity of a system in which the Food & Drug Administration (FDA) maintains processing oversight of a cheese pizza until pepperoni is added, at which point the oversight shifts to the U.S. Dept. of Agriculture’s Food Safety & Inspection Service (USDA FSIS).
There is near universal agreement that no one would design such a system if they were working off a proverbial clean sheet of paper. While this is undoubtedly correct, it forces us to juxtapose this theoretical point against the 100+ years of oversight, policy, and paperwork generated by the FDA, FSIS, and its predecessor agencies, not to mention other relevant players such as the Environmental Protection Agency (EPA), Centers for Disease Control & Prevention (CDC), and countless other state, local, and private parties. This history raises enormous practical and political barriers to change. We have a status quo maintained by a dizzying array of interests, both public and private, scattered through various government, departments, agencies, congressional committees, trade associations, labor unions, etc. Keep Reading
Except for those within food companies that are having their products routinely irradiated, we haven’t heard much about food irradiation over the last decade. However, recently there seems to be a resurgence of press articles and even government approvals related to irradiating food. What’s going on?
In the 1980s, the U.S. Food and Drug Administration (FDA) made a significant step by approving the irradiation of spices (more accurately, dehydrated aromatic vegetable substances) to a maximum dose limit of 30 kGy and fresh food products to a maximum dose limit of 1 kGy. These two applications are very different from one another and require different equipment. Furthermore, one is for perishable product and the other is for non-perishable product, requiring different product handling and logistics. Keep Reading
This blog was originally posted on FDAVoice on September 12, 2013.
On Sept. 6, FDA announced the results of testing 1,300 samples of arsenic in rice and rice products and found that the arsenic levels in rice do not present an immediate or short-term health risk. As we said last week, the next step is to assess the potential health risk from long-term exposure to the arsenic in rice and foods made with this grain.
And that is where my job starts. I am a scientist at FDA and I’d like to explain the scientific legwork that will be done over the next few months by some of the most preeminent arsenic experts in the country. Keep Reading
On August 10, the U.S. Dept. of Agriculture revised its estimated for this year’s corn crop, cutting it by nearly 17% due to the severe drought the United States experienced this spring and summer. And yet, this year’s corn harvest is expected to be perhaps the fifth largest on record. Recently, Kelly Hensel, IFT Digital Media Editor, spoke with Colin Carter, Professor of Agricultural and Resource Economics at the University of California, Davis, to get his insight on how techniques, including genetic modification, have helped U.S. farmers meet increasing demands under extreme weather variation. In addition, Carter addresses the concerns surrounding GM crops. Listen to the interview on IFT’s ePerspective blog and don’t forget to add your opinion to the dialog by commenting.
There has been a lot of media attention given to a product that is unfamiliar to most consumers, even though they have been eating it for the last 20 years. Lean finely textured beef, known by the derogatory term “pink slime,” has come to mean many things to many people. And as is often the case with something unfamiliar, people sometimes jump to conclusions that are based on incomplete facts.
Transgenic technology is a new high-tech tool developed by scientists to increase productivity and profitability of commercial food production, while at the same time increasing sustainability of food resources. Atlantic salmon is one example of such a nutritious limited food source. Our oceans cannot keep up with consumer demands for fish, a commodity that is not only highly sought after due to its culinary appeal, but is increasingly seen as healthy alternative to red meat. A transgenic line of Atlantic salmon (AquAdvantage salmon) was genetically engineered (GE) to grow faster by inserting an additional salmon growth hormone gene. The fast growth increases the annual output of aquaculture farms and also increases the efficiency of feed conversion (i.e., they need less food to produce the same amount of food compared with their slower growing, non-GE counterparts). Also, these GE-fish will be grown in contained, land-based facilities, preventing escape of the fish to the ocean and allowing general expansion of salmon aquaculture to meet growing demand without expanding the use of ocean net pens. Keep Reading