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    • D.C. Circuit to Hear COOL Case En BancApril 8th, 2014

      By Riëtte van Laack – Does the same standard that applies when regulators require label statements that “correct a deception,” such as false advertising, also apply when they require label statements for other purposes based on the interests of the government?  This issue will be before …

    • HP&M Comments on IND Guidance; Says FDA Lacks Authority to Impose Requirements on Non-drug StudiesApril 8th, 2014

      By Jennifer M. Thomas & James P. Ellison – Hyman, Phelps & McNamara, P.C. (HP&M) filed comments on April 7 concerning FDA’s Guidance document, Investigational New Drug Applications (INDs) — Determining Whether Human Research Studies Can Be Conducted Without an IND (the “Guidance”).  HP&M has previously blogged …

    • Registration Opens for ABA’s Fourth Annual Food and Supplements WorkshopApril 7th, 2014

      The American Bar Association’s Section of Ligation (specifically the Food and Supplements Subcommittee of the Products Liability Committee) just announced its Fourth Annual Food & Supplements Workshop, scheduled for June 5 in the Minneapolis area.  Among the topics to be addressed: Emerging Issues: Surveying the Regulatory …

    • Court of Appeals Affirms District Court’s Denial of Preliminary Injunction against COOL RegulationsMarch 31st, 2014

      By Riëtte van Laack – The U.S. Court of Appeals for the District of Columbia Circuit recently declined to stop USDA/AMS implementation of the amended Country of Origin Labeling ("COOL") regulations for beef, pork, and poultry products requiring identification of the country where the animals are …

    • Evaporated Cane Juice Case Evaporates (For Now)March 30th, 2014

      By Ricardo Carvajal – A putative class action targeting certain food products that declare “evaporated cane juice” (ECJ) as an ingredient was recently stayed based on the doctrine of primary jurisdiction.  As noted by the Court, prior decisions have gone both ways on the question of …

    • Like Spring, GMA Science Forum is Just Around the CornerMarch 30th, 2014

      GMA Science Forum 2014 kicks off on April 6 in Washington, DC.  The Forum will feature numerous sessions addressing scientific and regulatory issues of interest to the packaged food industry.  A complete agenda is available here.  HPM attorneys will help present a half-day introduction to …

    • Court Rules that FTC’s Substantiation Requirements Are Applicable to Claims for Medical FoodsMarch 12th, 2014

      By Riëtte van Laack – Defendants Wellness Support Network, and co-owners Robert and Robyn Held, marketed two diabetes products – Diabetic Pack and Insulin Resistance – as medical foods.  In 2005 and 2006, FDA issued two Warning letters to them (here and here), claiming the products …

    • Is That “Hummus” Really Hummus?March 11th, 2014

      By Ricardo Carvajal – Sabra Dipping Co., LLC ("Sabra") submitted a citizen petition (Dokcket No. FDA-2014-P-0259) asking FDA to establish a standard of identity ("SOI") for hummus.  The proposed SOI would define hummus as “the semisolid food prepared from mixing cooked, dehydrated, or dried chickpeas and tahini” with …

    • Amicus Filings in POM Wonderful’s Lanham Act Case Reflect Myriad of Views on Proper Interaction Between the FDC Act and Lanham ActMarch 10th, 2014

      By JP Ellison – We previously posted (here and here) about the Supreme Court case that will be argued next month in which the parties are debating the proper interplay between the Federal Food, Drug, and Cosmetic Act (“FDC Act”) and the Lanham Act.  Briefly, the issue …

    • A New Face for Nutrition Facts; FDA Proposes Major Revisions to the Nutrition Facts Box and Serving Size RegulationsMarch 2nd, 2014

      By Riëtte van Laack – Last week, FDA announced the long awaited proposal for revisions to the regulations (here and here) for the format and mandatory information included in the Nutrition Facts Box (“NFB”) and the Supplement Facts Box (“SFB”), and for the calculation of the …

    • Major Medical, Scientific, and Food Associations Object to FDA IND GuidanceFebruary 26th, 2014

      By Wes Siegner – The following organizations filed joint comments on November 26, 2013 voicing strong opposition to the food provisions of FDA’s final IND Guidance and requesting that FDA reopen the comment period to permit comment on the food provisions of the guidance, which FDA …

    • A New Front in the NGO Assault on GRAS: CFS Seeks a (Temporary?) Return to GRAS AffirmationFebruary 26th, 2014

      By Ricardo Carvajal, Diane B. McColl & JP Ellison – The Center for Food Safety filed suit in the DC District Court challenging FDA’s allegedly “unlawful action of exempting substances that are [GRAS] from regulation as food additives under a proposed rule for more than fifteen …

    • New Schedule Set for Issuance of FSMA RulesFebruary 21st, 2014

      By Ricardo Carvajal – FDA entered into a consent decree with the Center for Food Safety that specifies new deadlines for the agency’s submission of final rules implementing FSMA to the Federal Register for publication.  The consent decree marks the latest chapter in a case that …

    • FDA Publishes Draft Approach for Designating High-Risk FoodsFebruary 13th, 2014

      By Ricardo Carvajal – FDA published a notice announcing the availability of a Draft Approach for Designating High-Risk Foods, and asking for comments and information to help the agency refine that approach.  Designation of a food as a High-Risk Food (HRF) would trigger additional recordkeeping requirements intended …

    • FTC Files Brief in POM Wonderful LLC Appeal Arguing First Amendment Protection Is not Available for POM’s Allegedly Misleading ClaimsFebruary 10th, 2014

      By Riëtte van Laack – On Friday, February 7, 2014, the FTC filed its long-awaited brief in the D.C. Circuit action concerning POM Wonderful LLC’s (“POM’s”) advertising for its pomegranate products (see our previous post here).  Not surprising, the FTC asserts that POM’s ads were deceptive.  First, …