FDA Seeks Feedback on Fast-Track Product Permit Forms
Published Date: 9/21/2026
Notice
Summary
The FDA wants your thoughts on how they collect info for temporary marketing permits, which help companies get products to market quickly. This affects businesses applying for these permits and aims to keep the process smooth without extra costs or delays. You’ve got until November 20, 2026, to share your comments and help shape the rules!
Analyzed Economic Effects
4 provisions identified: 2 benefits, 2 costs, 0 mixed.
TMP application paperwork burden
If your food business files for a Temporary Marketing Permit (TMP) under 21 CFR 130.17(c), FDA estimates each response takes 25 hours. The table shows 2 responses per respondent (50 hours per respondent) and 13 respondents annually, for a total of 650 hours.
TMP extension paperwork burden
For requests to extend a TMP under 21 CFR 130.17(i), FDA estimates each response takes 2 hours. The table shows 2 responses for the (one) respondent, totaling 4 hours annually.
Guidance available for TMP applicants
FDA provides a guidance titled "Temporary Permits for Interstate Shipment of Experimental Packs of Food Varying from the Requirements of Definitions and Standards of Identity: Guidance for Industry" (November 2021) on its website to assist respondents with the TMP process.
No capital or O&M costs claimed
FDA states there are no capital costs or operating and maintenance (O&M) costs associated with this information collection for TMPs.
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Key Dates
Department and Agencies
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