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FDA Releases Final Rules Revising Nutrition Facts Label and Certain Serving Sizes; Industry Given Two to Three Years to Comply
  • Kelley Drye & Warren LLP
  • USA
  • May 20 2016

FDA announced today that it was finalizing two previously proposed rules that will require industry to overhaul Nutrition Facts panels on all food


FDA Releases Draft Guidance on Determining What Constitutes a “Qualified Facility” under FSMA Preventive Controls Rules
  • Kelley Drye & Warren LLP
  • USA
  • May 16 2016

On Friday, the FDA announced the availability of a draft guidance describing its current thinking on how to determine whether a business is a


Agree to Disagree? CFPB Rule Would Prohibit Mandatory Arbitration Clauses, Require Submission of Arbitral Records
  • Kelley Drye & Warren LLP
  • USA
  • May 11 2016

The Consumer Financial Protection Bureau released a proposed rule last week that would prohibit providers of consumer financial products and services


CFPB, “Please”: Judge Rebuffs CFPB’s Attempt to Compel Documents Regarding For-Profit College Accreditation
  • Kelley Drye & Warren LLP
  • USA
  • April 26 2016

Last Thursday, a federal district court judge in D.C. denied the Consumer Financial Protection Bureau's (CFPB) attempt to compel documents from the


FTC Releases Report on “Big Data” Offering Practical and Legal Considerations for Businesses
  • Kelley Drye & Warren LLP
  • USA
  • January 12 2016

On January 6, 2016, the Federal Trade Commission (FTC) released a report on the growing use of "big data" which discusses potential benefits and


FDA approves genetically engineered Atlantic salmon as safe and effective for human food and releases related draft guidance on voluntary labeling
  • Kelley Drye & Warren LLP
  • USA
  • November 24 2015

On Thursday, November 19th, the Food & Drug Administration (FDA) announced that it had approved an application for AquAdvantage Salmon, a type of


New FDA Guidance doubles-down on 1980 fortification policy and potential misbranding risks of “inappropriate fortification”
  • Kelley Drye & Warren LLP
  • USA
  • November 20 2015

FDA recently released its Guidance for Industry: Questions and Answers on FDA's Fortification Policy (Guidance) to "clarify the existing policy" in


FDA partially stays controversial policy of requiring INDs for clinical studies evaluating food, dietary supplements and cosmetics
  • Kelley Drye & Warren LLP
  • USA
  • November 10 2015

On Friday, October 30, 2015, FDA issued a Federal Register Notice announcing a partial stay of the agency's controversial Final IND Guidance entitled


CFPB obtains $13m FCRA settlement with employee background screening providers
  • Kelley Drye & Warren LLP
  • USA
  • November 10 2015

The CFPB recently initiated an enforcement action against General Information Services (GIS) and its affiliate, e-Background-checks.com, Inc. (BGC


FTC staff comment encourages FDA to reevaluate its current approach to regulating homeopathic products
  • Kelley Drye & Warren LLP
  • USA
  • August 24 2015

On Friday, staff of the Federal Trade Commission's Bureau of Consumer Protection, Office of Policy Planning, and Bureau of Economics submitted a