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The Daily Intake

Legal and Regulatory updates for the food and supplement industry

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FDA Announces Proposed Redesign to Create Human Foods Program

Posted on February 1, 2023
  • In light of the findings and recommendations of the external evaluation conducted by an expert panel at the Reagan-Udall Foundation (summarized here), FDA Commissioner Califf announced a proposed redesign
… Continue Reading FDA Announces Proposed Redesign to Create Human Foods Program

FDA’s Center for Food Safety and Applied Nutrition Continues Evaluation of Heavy Metals in Food and Child Development

Posted on January 13, 2023
  • On January 12, FDA’s Center for Food Safety and Applied Nutrition (CFSAN) released two press announcements regarding the Agency’s continued effort in addressing heavy metals in foods pursuant to its
… Continue Reading FDA’s Center for Food Safety and Applied Nutrition Continues Evaluation of Heavy Metals in Food and Child Development

External Evaluation of FDA’s Human Foods Program Published

Posted on December 7, 2022
  • As mentioned in July, FDA Commissioner Robert Califf commissioned an external evaluation of the FDA’s Human Foods Program (HFP), including the Office of Food Policy and Response (OFPR), the

…
Continue Reading External Evaluation of FDA’s Human Foods Program Published

FDA Evaluation of Agency Activities

Posted on July 21, 2022
  • On July 19, 2022, FDA Commissioner Robert Califf published a statement regarding FDA’s evaluation of agency activities. In his statement, Califf acknowledged that the agency has recently confronted challenges that

…
Continue Reading FDA Evaluation of Agency Activities

FDA Adds QR Code to Certain Food Export Certificates

Posted on June 23, 2020
  • Firms exporting food products from the U.S. are often required by foreign governments and companies to provide certain assurances regarding a product’s regulatory or marketing status in the U.S. The

…
Continue Reading FDA Adds QR Code to Certain Food Export Certificates

FDA Responds to Three Dietary Fiber Citizen Petitions

Posted on January 15, 2020
  • On January 10, the FDA announced that it intends to propose that “glucomannan” be added to the definition of dietary fiber at 21 CFR 101.9(c)(6)(i). Based on available evidence, FDA

…
Continue Reading FDA Responds to Three Dietary Fiber Citizen Petitions

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

FDA Provides Remarks on their Role in Supporting Innovation in Food Technology

Posted on March 28, 2018
  • On March 22, 2018, Susan Mayne, Ph.D., Director of FDA’s Center for Food Safety and Applied Nutrition, addressed the audience at the Future Food-Tech Summit about FDA’s role in supporting

…
Continue Reading FDA Provides Remarks on their Role in Supporting Innovation in Food Technology

FDA Announces Posting of Adverse Event Report Data for Foods and Cosmetics

Posted on December 7, 2016
  • FDA’s CFSAN Adverse Event Reporting System (CAERS) is a post-market surveillance system that contains information on adverse event and product complaint reports submitted to FDA for foods, dietary supplements, and

…
Continue Reading FDA Announces Posting of Adverse Event Report Data for Foods and Cosmetics

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Keller and Heckman, founded in 1962, has a broad practice in the areas of regulatory law, public policy, and litigation, serving both domestic and international clients. Our firm is a pioneer in the use of interdisciplinary approaches to problem-solving. Since 1971, we have had an in-house scientific staff that works closely with the firm’s attorneys on matters of technical complexity. Many of our attorneys also have government experience and expertise in multiple areas of the law.

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