Concept Nutrition, Inc.

Concept Nutrition, Inc. Lauren Swann, MS, RD, LDN, Consulting in Strategic Nutrition Communications, Food Labeling, Policy,
(1)

Strategies to effectively deliver accurate nutrition messages for the food industry, media and public health organizations

03/31/2026

FDA’s Office of Dietary Supplement Programs (ODSP) invites stakeholders to participate in a public meeting to discuss the evolving landscape of dietary suppl...

03/31/2026

The U.S. Food and Drug Administration is issuing a Request for Information today on a potential update to the acceptable market name for eighteen species of Sebastes, commonly known as rockfish.

Consumers often find marketing claims such as, raised without antibiotics, cage-free, and grass-fed on protein-based foo...
03/25/2026

Consumers often find marketing claims such as, raised without antibiotics, cage-free, and grass-fed on protein-based food packaging. USDA’s Agricultural Marketing Service (AMS) offers audit services that provide assurance to customers on the validity of these types of claims.
Through the USDA Process Verified Program (PVP), highly skilled AMS auditors confirm that a participating company is adhering to its own set of standards. This is a voluntary service, provided by AMS to give businesses a way to show products are in fact to the standard on their label.

Transparency from Farm to Market

03/24/2026

When you see this label, it means exactly what it says.

Born here. Raised here. Harvested here. Processed here. 🇺🇸

No shortcuts. No exceptions. No confusion.

That’s Product of USA.

🔗 www.productofusa.gov

the U.S. Fish and Wildlife Service proposes to amend the definition of “shellfish” in the Code of Federal Regulations (C...
03/06/2026

the U.S. Fish and Wildlife Service proposes to amend the definition of “shellfish” in the Code of Federal Regulations (CFR) by removing the phrase “having a shell” and adding specific taxa. This amendment would clarify that squid, cuttlefish, octopus, and other cephalopods are included within the regulatory definition of shellfish. This action is deregulatory in nature, as it reduces regulatory ambiguity, aligns the Service's regulations with current biological understanding and commercial practice, reduces regulatory burden and is within the Service's purview to amend definitions as needed.
Comments must be received or postmarked on or before April 6, 2026 and can be submitted electronically using the Federal eRulemaking Portal.

We, the U.S. Fish and Wildlife Service (Service), propose to amend the definition of "shellfish" in the Code of Federal Regulations (CFR) by removing the phrase "having a shell" and adding specific taxa. This amendment would clarify that squid, cuttlefish, octopus, and other cephalopods are...

March 27, 9:00am-3pm ET; in person or virtually; in-person meeting at U.S. Food and Drug Administration Wiley Auditorium...
03/03/2026

March 27, 9:00am-3pm ET; in person or virtually; in-person meeting at U.S. Food and Drug Administration Wiley Auditorium, 5001 Campus Dr, College Park, MD
FDA invites stakeholders to participate in a public meeting to discuss the evolving landscape of dietary supplement ingredients and how recent scientific and technological advances are shaping the industry; there will be presentations to provide background on:
- scope of the phrase “dietary substance for use by man to supplement the diet by increasing the total dietary intake” as used in DSHEA
- New methodologies to produce existing dietary ingredients
- Specific ingredient types, including proteins, enzymes, and microbials
will include an opportunity to provide oral comment for consideration; FDA will review input received at the public meeting and submitted to www.regulations.gov (docket number FDA-2026-N-2047) to determine next steps. Comments must be submitted on or before April 27, 2026.

The U.S. Food and Drug Administration is announcing a public meeting to be held on March 27, 2026, entitled “Exploring the Scope of Dietary Supplement Ingredie

FDA's list of guidance topics expected to publish as drafts or finals by the end of December 2026 includes possible new ...
02/16/2026

FDA's list of guidance topics expected to publish as drafts or finals by the end of December 2026 includes possible new topics or revisions to existing documents.
- Food Colors Derived from Natural Sources: Fruit Juice and Vegetable Juice as Color Additives in Food; Draft Guidance for Industry
- New Dietary Ingredient (NDI) Notifications and Related Issues: Identity and Safety Information About the NDI; Guidance for Industry
- Compliance Policy Guide for Determining the Identity, Quality, and Purity of Olive Oil and Olive-Pomace Oil Products; Draft Guidance for FDA Staff
- Food Labeling for Online Grocery Shopping Platforms; Draft Guidance for Industry
- Protein Efficiency Ratio (PER) Rat Bioassay Studies to Demonstrate that a New Infant Formula Supports the Quality Factor of Sufficient Biological Quality of Protein; Guidance for Industry

Possible new topics for guidance documents or revisions to existing guidance documents that the FDA Foods Program is considering.

02/11/2026

FDA Expert Panel on Food Allergies U.S. Food and Drug Administration sent this bulletin at 02/11/2026 08:44 AM EST If your email program has trouble displaying this email, view as a webpage. FDA Expert Panel on Food Allergies Wednesday, February 25, 2026, 1 - 3 p.m. ET The FDA Expert Panels are roun...

02/05/2026

As part of FDA’s efforts to Make America Healthy Again, the agency has worked with industry to phase out certain FD&C Act certified colors and has fast-tracked the approval of several naturally derived alternative colors.

"Companies will now have flexibility to claim products contain ‘no artificial colors’ when the products do not contain p...
02/05/2026

"Companies will now have flexibility to claim products contain ‘no artificial colors’ when the products do not contain petroleum-based colors. In the past, companies were generally only able to make such claims when their products had no added color whatsoever — whether derived from natural sources or otherwise. The agency sent a letter to industry providing notice of the FDA’s intent to exercise enforcement discretion related to these voluntary labeling claims."

Today, the U.S. Food and Drug Administration took additional steps to support the transition of our nation’s food supply from the use of artificial petroleum-based colors to alternatives derived from natural sources.

02/02/2026

BIG NEWS: U.S. Food and Drug Administration is taking action on food labeling that seeks to improve transparency in disclosures of ingredients that impact certain health conditions, such as gluten for those with celiac disease, and other established food allergens.

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Philadelphia, PA

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+12156391203

Website

http://www.linkedin.com/groups?home&gid=158141, http://www.linkedin.com/groups?home&gid=1

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