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Guidance 213 –
what will it mean
for producers?
Liz Wagstrom, DVM, MS, DACVPM
Chief Veterinarian, NPPC
FDA GUIDANCE #213
VFD RULE
FDA Guidance 213/VFD
• Guidance #213 finalized in 2014, VFD final
rule on June 2, 2015
• All manufacturers have agreed to comply
• Growth Promotion and Nutritional Efficiency
Labels will be removed by Dec. 2016
– “Medically Important”
• Disease Prevention, Control and Treatment
will be VFD in feed, Rx in water
FDA medically important
• All swine antibiotics will be affected under
Guidance 209 except
– Bacitracin*
– Carbadox
– Bambermycin
– Ionophores
– Tiamulin*
*Considered medically important by WHO list
These antibiotics will remain
available for growth promotion
and/or over-the-counter (OTC)
in feed and water
Industry Efforts - #213/VFD
• VFD negotiations with FDA
– Barnyard meetings
– Veterinarians and producers
– Producers to listening sessions
– Goal – make the VFD process more
workable
• Education and outreach to producers
and veterinarians
– Avoiding out of feed situations
– Avoiding enforcement actions
VFD Final Rule
Previous Rule
• 2 year record retention
• Original document to mill
• No extra-label use
• Order for tons of feed
• No refills, unless on label
• Written for one group of
animals on a premise
• VCPR required
Revised Rule
• 2 year record retention
• May email or fax document
• No extra-label use
• Order for number of days
• No refills, unless on label,
– Standing order?
• Attached list of premises
– For each mill
• State VCPR* required
• Max of 6 mo. expiration
Producer Impacts
• On Farm Feed Manufacturing
– Will not need to register as a distributor
unless producing feed for commerce
– Will need VFD to buy medicated premix (Type
B)
– Will not be able to have medicated feed in bin
after expiration of the VFD
Producer Impacts
• Likely most impactful to small producers or
those without a veterinarian
• Floor stock – will be legal but will it be
available
• Feed mill interpretation of rule
– Standing orders will be an issue
– Multiple groups during 6 months
– Pulse dosing of same group
Guidance 213/VFD Summary
• Most changes won’t be felt on farm
until manufacturers change labels
• Current VFD products now under the
new rule
• Label changes for others are required
by Dec, 2016
• Uncertain how many products will
change labels versus stop marketing
Next steps
• The FDA acknowledges the important role
medically important antimicrobials play in
treating, controlling, and preventing
disease in food producing animals
• Agency has been actively engaging
stakeholders to express our position that
medically important antibiotics labeled for
continuous or undefined durations of use
is not consistent with judicious use
principles
• In the case of disease prevention, the FDA
believes it is important such use is
appropriately targeted to animals at risk for
a specific disease and the use duration is
limited and risk-based
Disease Prevention
Disease Prevention
• NPB, NPPC, AASV Task Force
– Identified as major area to protect
– Identifying which products are at risk
– AASV – defining when prevention uses
appropriate (AABP and AAAP)
• Working with FDA to reinforce that
prevention is appropriate and necessary
to protect animal health
• USDA ARS research on production
practices
Conclusion
• Implementation of the rule will require a
collaborative effort
– Veterinarians, producers, feed manufacturers,
sponsor companies and FDA
• Compliance guidance written by FDA will
further clarify specific issues
• January 2017 should be really interesting!
Discussion?

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Dr. Liz Wagstrom - What Will Guidance 213 Mean To Producers For Antibiotic Use

  • 1. Guidance 213 – what will it mean for producers? Liz Wagstrom, DVM, MS, DACVPM Chief Veterinarian, NPPC
  • 3. FDA Guidance 213/VFD • Guidance #213 finalized in 2014, VFD final rule on June 2, 2015 • All manufacturers have agreed to comply • Growth Promotion and Nutritional Efficiency Labels will be removed by Dec. 2016 – “Medically Important” • Disease Prevention, Control and Treatment will be VFD in feed, Rx in water
  • 4. FDA medically important • All swine antibiotics will be affected under Guidance 209 except – Bacitracin* – Carbadox – Bambermycin – Ionophores – Tiamulin* *Considered medically important by WHO list These antibiotics will remain available for growth promotion and/or over-the-counter (OTC) in feed and water
  • 5. Industry Efforts - #213/VFD • VFD negotiations with FDA – Barnyard meetings – Veterinarians and producers – Producers to listening sessions – Goal – make the VFD process more workable • Education and outreach to producers and veterinarians – Avoiding out of feed situations – Avoiding enforcement actions
  • 6. VFD Final Rule Previous Rule • 2 year record retention • Original document to mill • No extra-label use • Order for tons of feed • No refills, unless on label • Written for one group of animals on a premise • VCPR required Revised Rule • 2 year record retention • May email or fax document • No extra-label use • Order for number of days • No refills, unless on label, – Standing order? • Attached list of premises – For each mill • State VCPR* required • Max of 6 mo. expiration
  • 7. Producer Impacts • On Farm Feed Manufacturing – Will not need to register as a distributor unless producing feed for commerce – Will need VFD to buy medicated premix (Type B) – Will not be able to have medicated feed in bin after expiration of the VFD
  • 8. Producer Impacts • Likely most impactful to small producers or those without a veterinarian • Floor stock – will be legal but will it be available • Feed mill interpretation of rule – Standing orders will be an issue – Multiple groups during 6 months – Pulse dosing of same group
  • 9. Guidance 213/VFD Summary • Most changes won’t be felt on farm until manufacturers change labels • Current VFD products now under the new rule • Label changes for others are required by Dec, 2016 • Uncertain how many products will change labels versus stop marketing
  • 10. Next steps • The FDA acknowledges the important role medically important antimicrobials play in treating, controlling, and preventing disease in food producing animals
  • 11. • Agency has been actively engaging stakeholders to express our position that medically important antibiotics labeled for continuous or undefined durations of use is not consistent with judicious use principles • In the case of disease prevention, the FDA believes it is important such use is appropriately targeted to animals at risk for a specific disease and the use duration is limited and risk-based
  • 13. Disease Prevention • NPB, NPPC, AASV Task Force – Identified as major area to protect – Identifying which products are at risk – AASV – defining when prevention uses appropriate (AABP and AAAP) • Working with FDA to reinforce that prevention is appropriate and necessary to protect animal health • USDA ARS research on production practices
  • 14. Conclusion • Implementation of the rule will require a collaborative effort – Veterinarians, producers, feed manufacturers, sponsor companies and FDA • Compliance guidance written by FDA will further clarify specific issues • January 2017 should be really interesting!