Nebraska cattle producers urged to prepare for the Veterinary Feed Directive regulations.

Nebraska beef cattle producers should begin preparing for the Jan. 1, 2017, implementation of the Veterinary Feed Directive regulations, according to Rob Eirich, Nebraska beef quality assurance director with Nebraska Extension. The regulations will be implemented by the U.S. Food and Drug Administration and will require producers to work directly with their veterinarian when they use feed-grade antibiotics with all food-producing livestock. A Veterinary Feed Directive is a paper or electronic written order by a licensed veterinarian approving the use of a feed-grade antibiotic for the prevention, treatment or control of a diagnosed disease. The regulations will apply only to antibiotics in livestock feed and will not affect feed-use medications such as ionophores, coccidia, other parasite and insect control drugs, or reproductive control medications. They also will not apply to antibiotics administered by injection. The first step producers should complete before January is to develop a valid Veterinarian Client Patient Relationship, which includes an operation site visit and discussion about herd health," Eirich said. "A complete herd health plan should be created for vaccination and treatment protocols during this discussion." Eirich said producers must look at their operation production calendar to determine what health risks they may encounter over the course of the year, how to prevent the risks through vaccinations and how to treat diagnosed diseases with antibiotics. This is an opportunity to look at alternatives to help reduce animal health risk, such as mineral programs or probiotic additives, he added. If a treatment protocol calls for using a feed-grade antibiotic, producers will be required to obtain a Veterinary Feed Directive from their veterinarian prior to purchasing and feeding the product. The veterinarian must provide signed written or electronic copies to the feed distributor and producer before the directive product is delivered to the producer. The directive must state what is being treated, the product used, rate of inclusion, duration of treatment, number of head being treated and at what location or operation. Each directive must also include an expiration date, which is the last date the product can be fed. Another key point for producers to understand, according to Eirich, is that the regulations allow no extra-label use of medicated feeds. These regulations will also be enforced more within the livestock industry, he said. Directive products can only be used for prevention, treatment or control of diseases indicated on the FDA Approved Labels.continue