AIC 2025 Application Form – AIC 2025

Registration

Please submit your application using the form below. Our team of administrators will review your submission.

Please allow 1–2 weeks for vetting once a complete application is submitted. Incomplete applications may take longer to process, so we recommend reviewing the requirements carefully before submission.

If you need any support or have questions, feel free to reach out to us at exhibiting@ifm.org. We’re here to help!

Basic Information

*Is your brand and/or booth name different than your company name? Please provide the brand/booth name that will appear on the promotional materials.


 

*This person is authorized to sign contracts on behalf of your company. 


 

*(name and role with company)

Please see our list of educators for reference: https://www.ifm.org/educators 

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*In the past five years, has your organization been cited, disciplined or identified by a regulatory body or in a public forum for unsubstantiated claims, conflicts of interest, or other citations that relate to reputational risk?


 

*By which regulatory agencies or organizations are you reviewed, accredited, certified, or regulated by, if applicable? Please indicate required vs optional.


 

*Disclaimer: If activities at your booth include lab testing, tests with rapidly available results and tests administered via venipuncture are not permitted. At home test kits are permitted, such as using single-use lancet, saliva, or cheek swab. Collections are not to be taken within the exhibit hall, but patients must be asked to collect the sample in the privacy of their room and return it to the lab company. All testing activities must adhere to local laws and regulatory requirements, and samples should be managed to maintain patient privacy/HIPAA. 


 

*Please provide URLs from your website or other method by which practitioners may access this evidence.

For proprietary products, devices, or unique clinical services only.


 

*Example: Vitamin D supplementation for male-pattern hair loss


 

*If applicable, provide a sample of practitioner or customer-facing documentation that explains the risk and any risk management strategies.


 

*Example: A sample patient-facing report with evidence.


 

* 1. The evidence should discuss clinical relevance (or relevance as a marker of dysfunction) for the given application. 2. Provide human evidence to support explicit claims for unconventional uses of commonly available assays. 

Example vitamin D testing as a marker of hydration status.


 

Check all that apply

Select all that apply

 
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Exhibitor Code of Ethics

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IFM's Code of Conduct

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