Proposed Rule 17 Jul 2025 compliance, fda, spices and flavorings, fruit juices, food grades and standards, seafood, consumer choice, food standards, food regulation, oils and fats, frozen foods, business flexibility

🍏Proposed Rule to Revoke Food Standards

The Food and Drug Administration (FDA or we) is proposing to revoke 23 standards of identity for food. FDA is taking this action because we tentatively conclude that these standards are no longer necessary to promote honesty and fair dealing in the interest of consumers. This proposed action would reduce redundant regulatory requirements.

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Rule 17 Jul 2025 business compliance, united states, fda, food grades and standards, food standards, food regulation

🍏FDA Revokes Obsolete Food Standards to Streamline Regulation

The Food and Drug Administration (FDA or we) revokes 11 food standards for foods that are no longer sold in the United States. FDA is taking this action as these standards are no longer necessary to promote honesty and fair dealing in the interest of consumers. This action will remove obsolete rules to reduce unnecessary regulatory requirements.

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Rule 12 May 2025 compliance, fda, medical devices, cosmetics, color additives, drugs, foods, food regulation, calcium phosphate

🍗FDA Approves Calcium Phosphate as Safe Color Additive

The Food and Drug Administration (FDA or we) is amending the color additive regulations to provide for the safe use of calcium phosphate as a color additive in ready-to-eat chicken products, white candy melts, doughnut sugar, and sugar for coated candies. This action is in response to a color additive petition (CAP) filed by Innophos, Inc. (Innophos or petitioner).

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Notice 1 May 2025 compliance, pharmaceuticals, fda, recordkeeping, export requirements, food regulation

📦FDA Export Notification and Recordkeeping Requirements Overview

The Food and Drug Administration (FDA, Agency, or we) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on information collection associated with notifications and records required for human drug, biological product, device, animal drug, food, cosmetic, and tobacco product exports.

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