July 14, 2020

Volume X, Number 196

July 14, 2020

Subscribe to Latest Legal News and Analysis

July 13, 2020

Subscribe to Latest Legal News and Analysis

FDA Reopens Comment Period on General Principles for Food Standards Modernization

As previously discussed on this blog, the U.S. Food and Drug Administration (FDA) held a public meeting on September 27, 2019, to give interested parties an opportunity to discuss FDA’s effort to modernize food standards of identity (SOI).  On February 20, 2020, FDA announced it plans to reopen the comment period on a 2005 proposed rule (which had initially been jointly published with the U.S. Department of Agriculture (USDA)) to establish a set of general principles for FDA to use when considering whether to establish, revise, or eliminate a food SOI. 

FDA is reopening the comment period to receive new data, information, and further comments only on FDA-specific aspects of the 2005 proposed rule (including 13 general principles for food standards modernization); however, FDA has indicated it will continue to engage with USDA before finalizing the proposed rule.

Food SOIs are regulatory requirements related to the content and production of certain food products such as milk (as previously discussed on this blog, FDA is particularly evaluating the use of the term, “milk,” in labeling plant-based products), breadjam, and chocolate.  As previously discussed on this blog, with the development of new types of food products and updated nutritional science, FDA is reconsidering SOIs as part of its Nutrition Innovation Strategy (NIS).

Written/electronic comments will be accepted for 60 days following the date of publication in the Federal Register.

© 2020 Keller and Heckman LLPNational Law Review, Volume X, Number 52


About this Author

Keller and Heckman offers global food and drug services to its clients. Our comprehensive and extensive food and drug practice is one of the largest in the world. We promote, protect, and defend products made by the spectrum of industries regulated by the U.S. Food and Drug Administration (FDA), the European Commission and Member States authorities in the European Union (EU) and similar authorities throughout the world. The products we help get to market include foods, pharmaceuticals, medical devices, veterinary products, dietary supplements, and cosmetics. In addition...