• where experts go to learn about FDA
  • Foods and Dietary Supplements

    • Court Rejects FTC’s Effort to Require Two StudiesJune 13th, 2012

      By Riëtte van Laack – As we previously reported, the United States District Court for the Southern District of Florida denied the Federal Trade Commission’s (“FTC’s”) motion to hold Garden of Life and its founder, Jordan S. Rubin (collectively “GOL”) in contempt for allegedly violating a court-issued …

    • Etched Citrus Coming Your Way!June 10th, 2012

      By Diane B. McColl -  The days of having to deal with those pesky adhesive labels on citrus fruit may be over.  FDA has announced a final rule approving the use of a carbon dioxide laser for etching information, such as product code, on the surface of …

    • A Sweet Day for SugarJune 1st, 2012

      By Ricardo Carvajal -  FDA denied a citizen petition submitted by the Corn Refiners Association ("CRA") which asked FDA to authorize the use of “corn sugar” as a common or usual name for high fructose corn syrup ("HFCS"), and to amend certain regulations that reference “corn …

    • House Passes FDA Reform Act of 2012; Next Up – Conference CommitteeMay 31st, 2012

      By Kurt R. Karst –       After a round of congratulatory speeches, the U.S. House of Representatives passed H.R. 5651, the FDA Reform Act of 2012, as amended, on May 30th by a vote of 387-5.  Unlike the U.S. Senate, which passed its version of the bill …

    • U.S. Senate Slogs Through Amendments and Passes FDA Safety and Innovation Act; Onward to the House BillMay 25th, 2012

      By Kurt R. Karst –       After days of debate and a slew of proposed amendments, the U.S. Senate passed S. 3187, the FDA Safety and Innovation Act, on Thursday afternoon by a roll call vote of 96-1.  Senator Bernie Sanders (I-VT), who cast the lone vote against passage, …

    • Initial Decision in POM Wonderful Case – Each Side Can Claim VictoryMay 21st, 2012

      By Riëtte van Laack – On May 21, 2012, the FTC posted the 345-page Administrative Law Judge’s ("ALJ’s") Initial Decision in In the Matter of POM Wonderful LLC et al. ("POM") (FTC Docket No. 9344).  The ALJ upheld the FTC’s Complaint insofar as the FTC asserted …

    • FSIS Proposes to Lift the General Prohibition against Sodium Benzoate, Benzoic Acid, and Sodium Propionate in Meat and PoultryMay 16th, 2012

      By Riëtte van Laack – Last week, the Food Safety and Inspection Service (“FSIS”) issued a proposal to lift the general prohibition against the use of sodium benzoate, benzoic acid, and sodium propionate in meat and poultry.  Historically, the use of these substances in meat and …

    • FSIS Finalizes Rules Mandated by the 2008 Farm BillMay 14th, 2012

      By Riëtte van Laack – On May 8, 2012, the Food Safety and Inspection Service (“FSIS”) published three sets of regulations mandated by the 2008 Farm Bill: (1) regulations requiring that meat and poultry plants promptly (within 24 hrs) notify FSIS that a contaminated or misbranded …

    • FDA Speaks to Nanotech in Cosmetics, Foods, and DrugsMay 14th, 2012

      By Ricardo Carvajal – April was a busy month for nanotechnology at FDA.  The agency issued two draft guidance documents worthy of close examination for those with an interest in the use of emerging technologies, including nanotechnology, in the cosmetic and food industries.  Further, FDA denied …

    • FSMA and the OMBMay 6th, 2012

      By Ricardo Carvajal – The Washington Post recently reported on the delay in getting clearance from the Office of Management and Budget (OMB) for the regulations that would implement the key provisions of the Food Safety Modernization Act.  Industry groups and consumer advocates purportedly are baffled, …

    • USP, Food Fraud, and FSMAApril 16th, 2012

      By Ricardo Carvajal – The USP plans to make available on its website a database of published articles that report “fraudulent activities related to food ingredients,” including foods used as ingredients (e.g., milk, honey, and olive oil).  The database will also be included in tabular format …

    • Sen. Durbin Asks FDA to Take Action Against (High Caffeine) Energy DrinksApril 11th, 2012

      By Riëtte van Laack – In an April 3, 2012 letter to FDA Commissioner Dr. Margaret Hamburg, Senator Richard Durbin (D-IL) requests that FDA take action against energy drinks containing “exceptionally high” levels of caffeine and other possibly stimulating substances such as guarana and ginseng.  Caffeine is …

    • Warning Letters Begin Addressing FSMA Reinspection FeesApril 9th, 2012

      By Ricardo Carvajal – Warning letters issued by FDA since late February provide an indication of the types of violations that could trigger reinspection fees under the authority provided by the Food Safety Modernization Act (“FSMA”).  As we noted in a prior blog posting, FSMA authorized …

    • FDA Denies NRDC’s Petition to Ban BPA in Food PackagingApril 3rd, 2012

      By Riëtte van Laack – On March 30, FDA denied a petition submitted by the Natural Resources Defense Council ("NRDC") to ban bisphenol A ("BPA") in food packaging.  As FDA explains in its 15-page response, the science NRDC presented in the petition was insufficient to support a conclusion …

    • NTP Director Turns Spotlight on Endocrine DisruptorsMarch 20th, 2012

      By Ricardo Carvajal –           Linda Birnbaum, Director of the National Institute of Environmental Health Sciences and the National Toxicology Program, published an editorial discussing the most recent evidence that certain environmental chemicals, including suspected endocrine disruptors such as BPA, “can have effects that would …