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The Daily Intake

Legal and Regulatory updates for the food and supplement industry

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Food Companies Agree to Phase Out Industrially Produced Trans Fat by 2023

Posted on May 14, 2019
  • As previously reported on this blog, the World Health Organization (WHO) released a plan in May 2018 aimed at eliminating industrially-produced trans fatty acids from the global food supply.

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Continue Reading Food Companies Agree to Phase Out Industrially Produced Trans Fat by 2023

FDA’s Quiet Reorganization of the Office of Food Additive Safety Begins Today

Posted on May 13, 2019
  • Before the Food and Drug Administration (FDA) took it down this morning, the website for the Office of Food Additive Safety (OFAS) showed three divisions for (1) Food Additive Petitions

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Continue Reading FDA’s Quiet Reorganization of the Office of Food Additive Safety Begins Today

Sharpless: ‘No Pause’ Following Gottlieb’s Departure

Posted on May 8, 2019
  • As previously reported on this blog, Ned Sharpless succeeded Scott Gottlieb as Acting FDA Commissioner in April 2019.  Prior to Sharpless’ tenure, it was unclear whether the agency would

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Continue Reading Sharpless: ‘No Pause’ Following Gottlieb’s Departure

FDA Announces “New Era of Smarter Food Safety”

Posted on May 1, 2019
  • On April 30, 2019, Acting FDA Commissioner Ned Sharpless, M.D., and Deputy Commissioner Frank Yiannas announced a “New Era of Smarter Food Safety,” an effort intended to combine

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Continue Reading FDA Announces “New Era of Smarter Food Safety”

CSPI Calls for National Registry of Gene-Edited Agricultural Crops

Posted on April 25, 2019
  • Criticizing the US Department of Agriculture (USDA) and Food and Drug Administration (FDA) for lack of oversight over foods produced with gene editing technology (e.g., Zinc Finger Nucleases, TALENS, or

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Continue Reading CSPI Calls for National Registry of Gene-Edited Agricultural Crops

FDA Issues Initiation of Voluntary Recall Draft Guidance

Posted on April 24, 2019
  • Today, FDA published a draft guidance on ways to prepare, plan, and work with the FDA to ensure voluntary recalls are initiated properly and timely. The draft guidance, titled “

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Continue Reading FDA Issues Initiation of Voluntary Recall Draft Guidance

FDA Allows Allulose to be Excluded From Sugar Declarations

Posted on April 19, 2019
  • On April 18, 2019, FDA released a draft guidance for industry entitled, “The Declaration of Allulose and Calories from Allulose on Nutrition and Supplement Facts Labels.” The guidance

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Continue Reading FDA Allows Allulose to be Excluded From Sugar Declarations

FDA Accepts Qualified Health Claim Petition for Yogurt and the Reduced Risk of Diabetes

Posted on April 18, 2019
  • FDA has accepted a qualified health claim petition submitted by Danone North America on the ability of yogurt to reduce the risk of type 2 diabetes.  FDA is accepting comments

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Continue Reading FDA Accepts Qualified Health Claim Petition for Yogurt and the Reduced Risk of Diabetes

FDA Announces New Tool to Alert the Public of Unlawful Ingredients in Dietary Supplements

Posted on April 17, 2019
  • As our readers may remember, earlier this year the FDA announced a plan for modernizing and strengthening dietary supplement regulation and oversight. Under the plan, the FDA stated their

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Continue Reading FDA Announces New Tool to Alert the Public of Unlawful Ingredients in Dietary Supplements

Despite Gottlieb’s Exit, FDA’s Nutrition Innovation Strategy Marches Forward

Posted on April 16, 2019
  • As previously reported on this blog, FDA’s Nutrition Innovation Strategy (NIS) is intended to improve public health via education regarding, and encouraging innovation in, the use of nutrition to promote

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Continue Reading Despite Gottlieb’s Exit, FDA’s Nutrition Innovation Strategy Marches Forward

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