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The Daily Intake

Legal and Regulatory updates for the food and supplement industry

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FDA Sued for Failure to Establish FSMA Accredited Labs Program by Statutory Deadline (subscription to Law360 required)

Posted on August 21, 2019
  • On August 19, two consumer groups, Center for Food Safety (CFS) and Center for Environmental Health (CEH), filed suit against the FDA in California federal court for its failure to

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Continue Reading FDA Sued for Failure to Establish FSMA Accredited Labs Program by Statutory Deadline (subscription to Law360 required)

FDA Proposes New Graphic Warnings for Cigarettes

Posted on August 16, 2019
  • The Federal Cigarette Labeling and Advertising Act (FCLAA), as amended by Section 201 of the Family Smoking Prevention and Tobacco Control Act (TCA; signed into law on June

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Continue Reading FDA Proposes New Graphic Warnings for Cigarettes

FDA Issues First Warning Letter to Food Importer Under FSVP

Posted on August 14, 2019
  • On August 13, FDA announced the issuance of the first warning letter to a U.S. food importer under the Food Safety Modernization Act’s (FSMA) Foreign Supplier Verification Program (FSVP).  As

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Continue Reading FDA Issues First Warning Letter to Food Importer Under FSVP

New Study Finds Prevalence of Sesame Allergy, as Illinois Becomes First State to Mandate Sesame Labeling on Packaged Foods

Posted on August 7, 2019
  • A new study by researchers from Northwestern University found that 0.49% of Americans, or 1.5 million children and adults, reported having an allergy to sesame, based on responses to a

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Continue Reading New Study Finds Prevalence of Sesame Allergy, as Illinois Becomes First State to Mandate Sesame Labeling on Packaged Foods

FDA Exploring Additional Regulatory Pathways for CBD Products

Posted on July 30, 2019
  • In testimony before the U.S. Senate Committee on Agriculture, Nutrition, and Forestry on July 25, FDA’s Principal Deputy Commissioner Amy Abernethy, M.D., Ph.D., reiterated that FDA “is committed to advancing

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Continue Reading FDA Exploring Additional Regulatory Pathways for CBD Products

FDA Suspends Topway/Kazy’s Gourmet Facility Registration

Posted on July 25, 2019
  • On July 22, 2019 the Food and Drug Administration (FDA) announced that it had suspended the food facility registration of Topway Enterprises, Inc, doing business as Kazy’s Gourmet of Houston,

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Continue Reading FDA Suspends Topway/Kazy’s Gourmet Facility Registration

FDA Announces FSMA Third-Party Certification Program User Fee Rates for Fiscal Year 2020

Posted on July 24, 2019
  • On July 23, 2019, FDA published a notice in the Federal Register announcing the fiscal year 2020 annual fee rate for recognized accreditation bodies and accredited certification bodies, and the

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Continue Reading FDA Announces FSMA Third-Party Certification Program User Fee Rates for Fiscal Year 2020

State AGs Want Role in Regulation of CBD-Containing Products

Posted on July 23, 2019
  • Many, including state regulators, are closely watching the U.S. Food and Drug Administration (FDA) as it works through the challenges associated with regulating cannabidiol (CBD) products.  Under the Federal Food,

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Continue Reading State AGs Want Role in Regulation of CBD-Containing Products

FDA Publishes Final Rule on Tolerances for Animal Drugs in Food

Posted on July 19, 2019
  • On July 10 FDA finalized its rule on Updating Tolerances for Residues of New Animal Drugs in Food.  This rule was originally proposed in 2012 with a revision proposed

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Continue Reading FDA Publishes Final Rule on Tolerances for Animal Drugs in Food

FDA Holds Ground in Challenge over GE Animal Regulatory Authority

Posted on July 12, 2019
  • As previously reported on this blog, on June 11, the President issued Executive Order Modernizing the Regulatory Framework for Agricultural Biotechnology Products, ensuring coordination across federal regulatory agencies

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Continue Reading FDA Holds Ground in Challenge over GE Animal Regulatory Authority

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