# 2025-13049: FDA Asks for Input on Emergency Med Product Data Gathering

2025-13049, Agency Information Collection Activities; Proposed Collection; Comment Request; Emergency Use Authorization of Medical Products, is a Federal Register notice from Health and Human Services Department, Food and Drug Administration published 2025-07-14, effective The notice allows 60 days for public comment on information collection activities related to Emergency Use Authorization under the Paperwork Reduction Act. (as of 2026-06-08).

- Canonical: https://policyrisk.com/federal-register/2025-13049
- As of: 2026-06-08
- Plain-text twin of the page above; the HTML and this file carry the same facts.

## Facts
- Document number: 2025-13049
- Title: Agency Information Collection Activities; Proposed Collection; Comment Request; Emergency Use Authorization of Medical Products
- Type: Notice
- Agencies: Health and Human Services Department; Food and Drug Administration
- Citation: 90 FR 31217
- Published: 2025-07-14
- Effective: The notice allows 60 days for public comment on information collection activities related to Emergency Use Authorization under the Paperwork Reduction Act.
- Comments close: not stated
- Significant: no
- Touches household money: no
- Regulation identifier numbers: none
- Last updated: 2026-06-08

## In one line

FDA Asks for Input on Emergency Med Product Data Gathering

## Summary

The FDA wants your thoughts on how they collect info about emergency use of medical products, like vaccines or treatments during health crises. This helps make sure the process is smooth and not too much paperwork for companies and the public. You’ve got 60 days to share your ideas, and this could affect how quickly lifesaving products get approved without extra costs or delays.

## Abstract

The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on information collection activities related to emergency use authorization for medical products.

## Effects PRIA read

No economic effects identified for this document.

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## Sources
- [2025-13049 on federalregister.gov](https://www.federalregister.gov/documents/2025/07/14/2025-13049/agency-information-collection-activities-proposed-collection-comment-request-emergency-use)
- [2025-13049 as published (PDF)](https://www.govinfo.gov/content/pkg/FR-2025-07-14/pdf/2025-13049.pdf)

## Related
- [Previous: 2025-13048, Determination of Regulatory Review Period for Purposes of Patent Extension; HEM…](https://policyrisk.com/federal-register/2025-13048)
- [Next: 2025-13050, Agency Information Collection Activities; Proposed Collection; Comment Request;…](https://policyrisk.com/federal-register/2025-13050)
- [All Federal Register documents](https://policyrisk.com/federal-register)

Source: PRIA, https://policyrisk.com/federal-register/2025-13049 (as of 2026-06-08).