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2027 AAFCO/FDA Quality Inspections Workshop Interest Survey

AAFCO and FDA are hosting an FDA-led workshop to be held in conjunction with AAFCO's 2027 Midyear Meeting. The workshop will provide foundational training for regulatory program managers and senior staff administrators on how to compile evidentiary documentation packages sufficient to support regulatory action. The training will include understanding FDA's legal authority and mission, federal jurisdictional requirements, and FDA 483 writing, as well as scenario-based exercises. To assist with planning, we are seeking feedback on what you'd like to takeaway from the workshop. Responses are due by October 31, 2026.

1.What is your current role?
Select the option that best describes your position.(Required.)
2.What state or federal regulatory agency do you represent?(Required.)
3.Are you currently planning to attend the 2027 Midyear Meeting?(Required.)
4.If this workshop were offered in conjunction with the 2027 Midyear meeting, how likely would you be able to attend the workshop?(Required.)
5.If you are a Program Manager, approximately how many staff members from your program would you be able to send to attend this workshop?
6.Would the availability of this workshop increase your likelihood of registering for the Midyear Meeting?(Required.)
7.What factors would affect your ability to participate?
Select all that apply. (Required.)
8.What topics or information would make this workshop most valuable to you?
9.Is there anything else you would like us to consider when determining how this workshop should be offered?
Thank you for completing the survey. We hope to see you at future AAFCO workshops and events!