Draft guidance for safety of animal feed clarified

FDA clarifies draft guidance for safety of animal feed on the farm

On March 19, the U.S. Food and Drug Administration issued a draft guidance, Guidance For Industry 203, to help animal producers take steps to help keep animal feed safe on the farm. The draft guidance outlines steps animal producers can take to identify feed contaminants that are sometimes present in the farm production environment and to prevent them from jeopardizing the health of farm animals and the safety of human food derived from the animals.

Draft guidance GFI 203 is intended to help animal producers identify:

  • Important animal feed safety issues that typically are not covered by regulations (e.g., unexpected changes in animal feed consumption patterns that could indicate the presence of contaminants in the feed; or contaminants that may be present in bedding or fencing materials that animals might eat)

  • A comprehensive approach to feed safety at the farm, beginning with acquisition of safe feed and maintenance of its safety until the feed is offered to animals. “Farm” means animal production units (e.g., integrated poultry grower operations, swine finishing units, cattle feedlots)

The draft guidance does not address the manufacture of feed on farms.

The FDA’s guidance documents, including guidance GFI 203, do not establish legally enforceable responsibilities. Instead, guidance describe the agency’s current thinking on a topic and provide recommendations, unless specific regulatory or statutory requirements are cited. The use of the word “should” in FDA guidance means that something is suggested or recommended, but not required.

The FDA is accepting public comments on this draft guidance through June 3. While comments are welcome at any time, you should submit them by June 3 in order for the FDA to consider your comments in drafting the final guidance.

To submit your comments electronically to the docket, go to www.regulations.gov and type FDA-2014-D-1180 in the search box.

To submit your comments to the docket by mail, use: The Division of Dockets Management, HFA-305, Food and Drug Administration, 5630 Fishers Lane, Room 1061, Rockville, MD 20852.

Be sure to include docket number FDA-2014-D-1180 on each page of your written comments.

Hide comments

Comments

  • Allowed HTML tags: <em> <strong> <blockquote> <br> <p>

Plain text

  • No HTML tags allowed.
  • Web page addresses and e-mail addresses turn into links automatically.
  • Lines and paragraphs break automatically.
Publish