FDA Foods Program Releases Guidance Topics
Posted in Legal Bites
FDA Foods Program Releases Guidance Topics

On June 29, 2021, the U.S. Food and Drug Administration’s (“FDA”) Center for Food Safety and Applied Nutrition and Office of Food Policy and Response released a list of draft and final guidance topics that are a priority for the FDA Foods Program to complete during the next 12 months. 

The FDA anticipates publishing guidance for many of these documents by June 2022. The FDA stated that the agency “is taking this action to provide stakeholders increased transparency and additional insights into the foods program priorities. Guidance documents represent the FDA’s current thinking on a specific topic and the information can help stakeholders plan for potential changes that may impact their businesses and organizations. They do not impose legally enforceable requirements.”

The FDA further stated that in the future the agency “intends to release the list of anticipated human food and cosmetic guidance topics at the beginning of each calendar year with updates scheduled for mid-year.” The list released on June 29 will be updated by the end of January 2022.

The guidance topics announced include:

  • Evaluating the public health importance of food allergens other than the major food allergens
  • Questions and answers regarding food allergens
  • Policy regarding certain new dietary ingredients and dietary supplements subject to the requirement for pre-market notifications
  • Best practices for convening a GRAS panel
  • Action levels for lead in juice
  • Lead action levels for categories of foods consumed by babies and young children
  • Prevention of salmonella enteritidis in shell eggs during production
  • Reducing microbial food safety hazards in the production of seed for Sprouting
  • Labeling of plant-based milk alternatives
  • Voluntary sodium reduction goals: target mean and upper bound concentrations for sodium in commercially processed, packaged and prepared foods

Public comments on the guidance can be submitted to www.regulations.gov.

Tags: FDA
  • Pooja S. Nair
    Partner

    Pooja S. Nair is a Partner and Chair of the Food, Beverage and Hospitality Department.

    Pooja S. Nair is a business litigator with a proven track record of delivering creative, effective, and long-term solutions to complex legal ...

Subscribe

Recent Posts

Blogs

Contributors

Archives

Jump to PageX

Ervin Cohen & Jessup LLP Cookie Preference Center

Your Privacy

When you visit our website, we use cookies on your browser to collect information. The information collected might relate to you, your preferences, or your device, and is mostly used to make the site work as you expect it to and to provide a more personalized web experience. For more information about how we use Cookies, please see our Privacy Policy.

Strictly Necessary Cookies

Always Active

Necessary cookies enable core functionality such as security, network management, and accessibility. These cookies may only be disabled by changing your browser settings, but this may affect how the website functions.

Functional Cookies

Always Active

Some functions of the site require remembering user choices, for example your cookie preference, or keyword search highlighting. These do not store any personal information.

Form Submissions

Always Active

When submitting your data, for example on a contact form or event registration, a cookie might be used to monitor the state of your submission across pages.

Performance Cookies

Performance cookies help us improve our website by collecting and reporting information on its usage. We access and process information from these cookies at an aggregate level.

Powered by Firmseek